Abstract
The American chestnut (Castanea dentata, 2n = 2x = 24), once known as the “King of the Appalachian Forest”, was decimated by chestnut blight during the first half of the twentieth century by an invasive fungus (Cryphonectria parasitica). The Chinese chestnut (C. mollissima, 2n = 2x = 24), in contrast to American chestnut, is resistant to this blight. Efforts are being made to transfer this resistance to American chestnut through backcross breeding and genetic engineering. Both chestnut genomes have been genetically mapped and recently sequenced to facilitate gene discovery efforts aimed at assisting molecular breeding and genetic engineering. To complement and extend this genomic work, we analyzed the distribution and organization of their ribosomal DNAs (35S and 5S rDNA), and the chromatin composition of the nucleolus organizing region (NOR)-associated satellites. Using fluorescent in situ hybridization (FISH), we have identified two 35S (one major and one minor) and one 5S rDNA sites. The major 35S rDNA sites are terminal and sub-terminal in American and Chinese chestnuts, respectively, originating at the end of the short arm of the chromosome, extending through the secondary constriction and into the satellites. An additional 5S locus was identified in certain Chinese chestnut accessions, and it was linked distally to the major 35S site. The NOR-associated satellite in Chinese chestnut was found to comprise a proximal region packed with 35S rDNA and a distinct distal heterochromatic region. In contrast, the American chestnut satellite was relatively small and devoid of the distal heterochromatic region.
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Introduction
Chestnuts belong to the genus Castanea, which consists of seven diploid (2n = 2x = 24) species native to temperate regions of the northern hemisphere1,2. The American chestnut [Castanea dentata (Marsh.) Borkh.], once known as the “King of the Appalachian Forest”, grew on over 800,000 km2 in its native range in eastern North America until its decimation by chestnut blight [caused by Cryphonectria parasitica (Murr.) Burr.] in the first half of the twentieth century. At one-point, American chestnut produced up to 25% of the hardwood lumber volume in the northeastern area of the United States and up to 15% in the Appalachian Mountains3,4,5,6. Chestnuts (Castanea spp.) are one of the most useful trees in the world, providing reliable, high carbohydrate food sources, stunningly beautiful, rot-resistant wood, and high-quality tannins for leather production5,6,7.
Chestnut blight is considered the worst man-made disaster in the history of the world’s forest ecosystems and directly resulted in the passage of the Plant Quarantine Act enacted by the United States Government in 1912 to reduce the chances of such a catastrophic event happening again8. The blight fungus was accidentally introduced in the late nineteenth century when chestnut seedlings from Japan were imported for commercial purposes9,10. The disease was first identified at the Bronx Zoo, New York, in 190411,12, and in a span of about 50 years, some four billion American chestnut trees were lost to blight13,14. In contrast to American chestnut, Chinese chestnut (C. mollissima Blume) co-evolved with the pathogen and is resistant to chestnut blight15. Soon after the devastating impact of chestnut blight was realized, scientists began hybridizing Asian chestnuts with American chestnut to develop a blight-resistant chestnut for replanting16,17. Over the past few decades and especially more recently, interspecies backcross breeding and genetic engineering have been implemented collaboratively by the American Chestnut Foundation (TACF), the State University of New York, College of Environmental Science and Forestry (SUNY-ESF)17,18,19, and various forest health researchers and partners, with the goal of restoring American chestnut to its native range16.
Genetic linkage and physical maps have been developed for Chinese chestnut20,21,22,23 to identify and locate disease resistance genes for blight and Phytophthora root rot. In addition, Chinese chestnut genomes have been sequenced and assembled24,25,26,27, as has the American chestnut genome28. Unlike the comprehensive genome analysis (mapping, karyotyping, and sequencing) conducted in some plant species [e.g., Arabidopsis29,30, rice31, sorghum32, maize33, tomato34, wheat35, less has been done to study the chestnut genome, especially with respect to cytogenomics (molecular cytological analysis). Cytogenomic research complements genetic mapping and genome sequencing by detecting structural rearrangements such as inversions and translocations, which are common features between related species and their hybrids33,36,37,38. This knowledge is important for inter-species hybrid breeding especially if the target gene(s) are located on rearranged chromosome(s).
Fluorescence in situ hybridization (FISH), a cytogenomic technique to visualize specific DNA sequences in cells, has played an important role in revealing the structural organization and evolution of genomes, including localizing markers and/or genes to specific chromosomes31,32,39,40,41,42,43,44,45. In plants, ribosomal DNAs (rDNA) consisting of 18S–5.8S–25S/26S rDNA (referred to as 35S rDNA) and 5S rDNA occupy specific regions on one or several chromosomes of a genome. The major 35S rDNA associated with the nucleolus is in the NOR (nucleolus organizing region) and is often visually apparent as a secondary constriction, the primary constriction being at the centromere. The regions distal to the secondary constrictions are termed satellites and they can vary in size46. The rRNA genes within the 35S and 5S rDNA are arranged in tandem repeats of a few to several hundred or even thousands of copies47 and are often used as unique cytogenomics landmarks in FISH for karyotype analysis and studies of genome organization. In addition, their copy number variation and cytological positions on chromosomes provide evolutionary insight into relationships among species and the speciation process36,48,49,50,51,52,53.
To complement and extend the available genome information for American and Chinese chestnuts, we conducted a detailed cytogenomic characterization of the rDNA loci and their associated satellites in these species as well as their interspecific hybrid. Our specific objectives were as follows:
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(i)
to determine and compare the distribution and organization of the ribosomal gene loci (35S and 5S rDNAs) in American and Chinese chestnuts, and
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(ii)
to characterize and compare the structural phenotype, and chromatin composition of their NOR (35S rDNA)-associated satellites.
Results
Precis of results
One American chestnut (AC) and four Chinese chestnut accessions (CC1, CC2, CC3 and CC4) were analyzed for the occurrence of rDNA by FISH. Chromosome spreads of enzymatically digested root tips, mostly free of cell walls, nuclear membranes, and cytoplasmic debris, with well-separated chromosomes, provided good conditions for FISH54,55. The chromosomal morphology of all accessions was similar. Each accession has metacentric (m), near-metacentric (nm) and sub-metacentric (sm) chromosomes, and a NOR-associated satellite pair (see Supplementary Fig. S1A). Images for the chromosome spreads and an accompanying illustration of the morphology of the chromosomes containing rDNA loci for each accession are shown in Fig. 1 for AC and in Figs. 2, 3, 4, 5 for CC1 to CC4, respectively. Figure 6 presents a diagrammatic illustration of the major 35S rDNA bearing chromosome of AC and the North American accessions (NAAs) of Chinese chestnut, and the second 5S rDNA site in two NAAs (CC3 and CC4). Figure 7 shows GISH (genomic in situ hybridization) results for the F1 hybrid. Based on physical appearance we observed two different sizes of the satellites in CC3 and CC4, referred hereafter as SAT-1 for the larger of the pair and SAT-2 for the smaller (see Supplementary Fig. S1B). Additional FISH images and diagrammatic illustrations are presented in Supplementary Figures S2 to S7. A comprehensive summary is available in Supplementary information 2 (PowerPoint slides), 3 (PowerPoint slides' narratives), and 4 (PowerPoint audio-video presentation). Throughout the results and discussion, the 35S rDNA and 5S rDNA will be referred as 35S and 5S, respectively. In addition, the major 35S rDNA as mj-35S and the minor 35S rDNA as mn-35S.
Ribosomal DNA in American and Chinese chestnuts
In the American chestnut (AC) two 35S sites (one major site and one minor site) and one 5S site (Fig. 1) were independently located on three different chromosomes. The mj-35S locus was located terminally with the FISH signal covering the end of the short arm of its chromosome, the secondary constriction (SC), and the entire satellite (Fig. 1a, double arrows). The mn-35S (Fig. 1a, green signals, arrows) and the 5S (Fig. 1a, red signals, arrowheads) sites were located proximally on the short arms. The signal intensity for the mj-35S appeared monomorphic on both homologues. In contrast, the signal intensities of the mn-35S and the 5S were dimorphic, that is, more intense for one homologue than for the other.
In Chinese chestnut CC1, we observed the same number of 35S and 5S loci (Fig. 2a) as in AC. Nevertheless, compared to AC the CC1 satellite was larger [Fig. 2a (encircled), an enlarged image (processed further) shown in upper-right corner], with its proximal half covered by the mj-35S green signal and distal half stained intensely with DAPI. In addition, these satellites appeared to be completely detached from their mother chromosomes (Fig. 2a, double arrows, middle-left). The mn-35S (Fig. 2a, double arrowheads) and the 5S (Fig. 2a, arrows) loci were observed in the same positions as in AC (compare Figs. 1a and 2a). All three of the rDNA loci appeared dimorphic in signal intensity.
Our result in CC1, namely the mj-35S locus mapping distal to the centromere (i.e., sub-terminal position), differs from a previous analysis of Chinese chestnut56, where the mj-35S locus was in a pericentromeric position. Given this observed difference, we analyzed three additional unrelated NAAs of Chinese chestnut, CC2, CC3 and CC4, and compared them to CC1 and AC. Interestingly, the four NAAs of Chinese chestnut (NAAs CC) did not differ in the position of the mj-35S locus but did vary in satellite length (see Supplementary Fig. S1B) and DNA composition. For additional details, see the animated and automated PowerPoint presentation, its accompanying narratives and the PPT audio-video in Supplementary information 2, 3 and 4, respectively. On one homologue of CC3 the mj-35S signal completely covered the SC and the satellite as in AC (Fig. 3a,b,d,e, double arrowheads, and Supplementary Figs. S4 and S5). The signal intensity of the mj-35S rDNA probes, which is monomorphic for the AC homologues (Fig. 1a,c, green signals, double arrows), is dimorphic for all Chinese chestnuts studied as illustrated in Fig. 2a (CC1), Fig. 2d (encircled middle-center, CC2), and 2e (enlarged image insert top-left, CC2), Fig. 3a,b,d,e (CC3) and Fig. 4a,c (CC4). Chromosomal positions for the mn-35S and the 5S sites for all NAAs of CC were similar as AC, including being dimorphic in their signal intensities. An additional 5S rDNA site in CC3 and CC4, located on the NOR-associated satellite, was observed linked distally to the mj-35S rDNA. Chinese chestnut accession CC3 was heteromorphic for this second 5S rDNA site as a single homologue exhibited the FISH signal [Fig. 3a1,a3,a4, (red signal, inserts top), and Fig. 5a2–a4,b (box, top-right), Fig. 5b1,b3 (red signal, arrow)] while signals were detected on both homologues of CC4 [Fig. 4a,b (red signals, double arrowheads)].
The chromosome spreads of American chestnut (AC) were highly condensed metaphase cells (Fig. 1) with a highly condensed NOR and associated satellite. The Chinese chestnut spreads (CC1, CC2, CC3 and CC4) were in pro- and early-metaphase stages with moderately condensed NORs. An intact stretched NOR can be clearly seen in early metaphase spreads [Fig. 3e (CC3) and Fig. 7 (F1 hybrid)]. As mentioned, the satellites of CC1 and CC4 do not appear to be associated with their mother chromosomes as there is little visual evidence they are connected. In addition, there is no 35S rDNA signal extending from the mother chromosomes of CC1 (Fig. 2a, double arrows, middle-left) to the satellites (encircled, middle of the image). However, several scattered 35S signals are visible in CC2 (Fig. 2d, red) when the image is enhanced, showing the path of the NOR that connects the respective mother chromosome to its satellite (Fig. 2e, white dotted lines along with arrowheads). This connection is clearly apparent in a slightly more condensed chromosome spread of CC3 where the mj-35S signal beginning on the short arm of the chromosome, passes through the SC and then extends into the proximal region of the SAT-1 (Fig. 3b, box), and completely covers SAT-2 (Fig. 3b, double arrowhead). Furthermore, when the spread quality was good, both chromatids at the NOR could be detected in mid- or late-prophase (or early pro-metaphase) as shown in Supplementary Fig. S5 and Supplementary information 2 and 4 (slide No. 3). The differences between Chinese and American chestnut revealed by FISH of mj-35S rDNA are summarized in a diagrammatic illustration in Fig. 6.
Satellites of American and Chinese chestnuts
The satellites of American chestnut and all studied NAAs of Chinese chestnut (CC1, CC2, CC3 and CC4) were unique in their physical size and chromatin composition. In AC, the mj-35S signals covered the NOR and the satellite (Fig. 1a, double arrows). An enlarged image indicates the signal extended from above the satellite into the short arm of the chromosome proximal to the NOR (Fig. 1d, and Supplementary Fig. S3a–d). When the 35S signal was removed through image analysis, a small satellite was visible as a less intense DAPI stained region [Fig. 1b (double arrowheads), Fig. 1e (arrowheads in white dotted circle), and Supplementary Figs. S2e1 (insert, bottom), S2e2 (insert, third right), S3f (arrowheads in white dotted circle and arrowheads in rectangular box)]. Since the satellite is completely covered by the mj-35S signal, there was a question as to whether the satellite was intact. To answer this question, we used the ATRS (i.e., telomere) probe in FISH in addition to the 35S probe. We observed a pair of telomere signals (red, Fig. 1c) at the end of each chromosome, including the ends of the satellites under a Cy3 filter (Fig. 1c, arrowheads, inserts). This confirmed the integrity of the chromosomes.
Unlike AC satellites, which appeared to be euchromatic, satellites of CC1, CC2, CC3 and CC4, except for one homologue of CC3, appear to be composed distally of heterochromatin and proximally of euchromatic DNA, which is apparent in Fig. 5a and illustrated in Fig. 6. This distinction, euchromatic vs. heterochromatic regions, is clearly observed in early- and mid-prophase cells, and at times in late-prophase or early pro-metaphase cells (CC4, Fig. 4f4,f8) with appropriate chromatin condensation and DAPI stain. The chromatin composition is clearly visible in Fig. 2f for CC2, where the less intense DAPI stain is indicated by braces in the upper right inset while the intense DAPI staining identifying heterochromatin is indicated by the circled region (the distal half of the satellite). The CC4 satellites differ in size (Fig. 4f; see Supplementary Fig. S1B), with one satellite being slightly larger (SAT-1) than the other (SAT-2). The CC3 satellites were unique with SAT-2 being similar to AC, small and nearly invisible unless the image was processed further (i.e., by enhancing the blue channel) [Fig. 3c, an enhanced DAPI image (arrowhead), Fig. 3d4 (insert), Fig. 3e4 (insert)], while SAT-1 was like the other Chinese chestnut NAAs [Fig. 3a5 (an enlarged DAPI image), Fig. 3c (dotted box), Fig. 3d2 (insert), Fig. 3e2 (insert)].
Ribosomal RNA genes and the proximal region of the satellite
To locate the mj-35S and the second 5S rDNA more precisely, we completed additional analyses using interphase nuclei and a prophase cell of the NAAs of Chinese chestnut. The enlarged image of a mid-prophase cell of a CC3 satellite (SAT-1) is shown in Fig. 5a1–a6. The mj-35S signal was very intense, obscuring a large portion of the satellite (the proximal half), but when removed through image processing, the chromatin composition becomes more apparent. The distal half of the satellite, composed of AT-rich heterochromatin that fluoresced intensely with DAPI under a blue filter [Fig. 5a5 (encircled), arrow in b4, c2, c4]. In contrast, the proximal half, which fluoresced less intensely [Fig. 5a6 (white dotted outlined), Fig. 5c2 (brace), Fig. 5c4 (brace)], might be euchromatic. The interphase nuclei of all NAAs of Chinese chestnut showed a characteristic spherical heterochromatic body [Fig. 5b, (SAT-1 of CC3, white dotted box), Fig. 5c (SAT-1 and SAT-2 of CC4, two white dotted boxes)], which is the distal portion of the satellite. The orientation of the mj-35S signals in CC4 (polar-side view, Fig. 5c1, SAT-1) obscured the spatial relationship of mj-35S rDNA and the satellite; however, the orientation of the SAT-2 (side view, Fig. 5c3) made it possible to determine unambiguously that the 35S rRNA genes were only in the weakly DAPI stained region of the satellite and clearly not in the heterochromatic region. Similarly, the second 5S rRNA locus in CC3 was definitely not associated with the heterochromatic region of SAT-1 [Fig. 5b3, also see Supplementary information 2 and 4 (slide No. 6)].
The mj-35S rDNA genic region was highly decondensed in interphase nuclei, as indicated by dispersed signals [Fig. 5b (green), and Supplementary Fig. S2c (red)], and are not associated with the heterochromatic region of the satellite (Fig. 5c4, arrow). The dispersed mj-35S signals along with or without the 5S rDNA locus coalesced as chromatin condensation progressed, revealing a visible connection of the mother chromosome to the satellite (Figs. 2e, 3b,d and Supplementary Figs. S2, S4 and S5).
American × Chinese chestnut interspecific hybrid
In the interspecific F1 hybrid, chromosomes of American and Chinese chestnut could not be distinguished solely with GISH. Pericentromeric heterochromatic regions of some of the chromosomes were more densely covered by green hybridization signals (Fig. 7a), but it was not sufficient to determine the lineage of each chromosome (see review by Schubert et al.57). However, combining GISH with 35S rDNA FISH probes confirmed this cell was from an interspecific hybrid. This hybrid provided a unique opportunity to examine the compositional differences of the parental satellites under the same biological and cellular conditions. Consistent with previous observations, the mj-35S rDNA bearing chromosome of Chinese chestnut had a distinct portion of the satellite (bright green signal in GISH) extending beyond the 35S rDNA signal (Fig. 7a, mj-35S CC, red) that is heterochromatic, while the American chestnut’s satellite was completely covered by the signal (Fig. 7a, mj-35S AC). The DNA of each satellite was unique, as the genomic DNA of Chinese chestnut (GISH probe) hybridized to its satellite [bright green signal, Fig. 7a (boxes, top-left), Fig. 7b1,b2]; but a very limited hybridization occurred on the American chestnut satellite (Fig. 7b6, a few greenish dots of hybridization signals). Moreover, in the Chinese chestnut satellite, the distal region showed a strong DAPI stain, while the proximal region had a weaker stain and hybridized with the 35S rDNA. This indicates that the distal region is highly heterochromatic and noticeably distinct from the proximal region (as marked by dotted line in Fig. 7a, top-left box; and Fig. 7b1). Additionally, the middle segment of the NOR, which is the secondary constriction (SC), displayed no DAPI staining, meaning that it is DAPI negative (Fig. 7b2). This suggests that this region has a high GC content.
Discussion
The number of rDNA loci (35S and 5S) and their organization with respect to copy numbers and chromosomal locations vary between and within species. This has led to their use for studying the chromosome structure and evolution of eukaryotic organisms36,51,58,59,60,61,62,63,64,65.
Ribosomal DNA variation
We observed two 35S loci in both American and Chinese chestnuts, while the number of 5S loci varied. The American chestnut, as well as two NAAs of Chinese chestnut (CC1 and CC2) each had one 5S locus. Similar results have been reported in Japanese chestnut [C. crenata (Siebold & Zucc.)] and European chestnut [C. sativa (Mill.)]56. However, CC3 and CC4 had an additional 5S locus on the satellite linked distally to mj-35S. Gain or loss of a ribosomal locus is a common evolutionary feature in speciation48,66. The mj-35S site in AC was located at the terminal position, and those in the NAAs CC were located at the sub-terminal positions except for one homologue of CC3 located terminally. This homologue with terminal mj-35S may be pre-existent in the ancestral background of this accession’s maternal parent (i.e., ‘AU-Cropper’) or CC3 may represent a hybrid pollinated either by C. crenata or C. sativa since these two species were grown in the same orchard in Missouri with ‘AU-Cropper’. This would be consistent with Ribeiro et al.56, who found that both C. crenata and C. sativa carry a terminal mj-35S rDNA site. Interestingly, our results for the NNAs CC differ from that of Ribeiro et al.56, where the mj-35S and the second 5S loci in the European accession of C. mollissima were pericentromeric on the short arm. These authors suggested that these rDNA loci had been restructured during the evolution of Castanea species.
Our results agree with the FISH characterization of 11 Quercus species (members of the same family, Fagaceae) including Q. robur59, which was separated within the Fagales clade at about the same time (13.62 Mya) as C. mollissima27. An expressed sequence tag-consensus map between Q. robur and C. sativa67 further supports evolutionary relatedness between Q. robur and Castanea as does comparative mapping presented in Staton et al.24. Phylogenetically, Quercus and Castanea are closely related68,69, and molecular data suggested that C. mollissima was the first Castanea to evolve followed by C. crenata, C. sativa, and C. dentata70. Castanea mollissima may be a mosaic of land races derived from small founder populations in multiple domestication events combined with serial transfer of selections from one location to another, again with small founder populations. Under this scenario, the European accession of C. mollissima56 and the NAAs CC in our study would have presumably originated from different landraces. Based on this interpretation, it appears the European accession is likely to be a more recent derivative than the NAAs CC studied here and might have apparently resulted from a structural rearrangement of the mj-35S rDNA bearing chromosome through an inversion, translocation, or breakage-fusion event (for details see Supplementary information 1 and Supplementary Fig. S7).
In most eukaryotes the 35S (or 45S in animals) and the 5S rDNA loci are located independently of each other (known as S-type arrangement) and are rarely co-localized or linked (known as L-type association). In C. mollissima, we observed both L- and S-type associations. The L-type association was reported in only about 9% of 1791 plant species studied (see review by Garcia et al.47) and the 35S locus was predominantly distal to 5S, which is the reverse of what we found in accessions CC3 and CC4 where the 35S site was proximal to the 5S. Based on our FISH image analyses we suggest two possible scenarios of the L-type association of the 35S and 5S genes in chestnut. First, the distal portion of the 35S gene overlaps the proximal segment of the 5S gene (see Fig. 4a). Second, the 5S gene is embedded in the distal portion of the 35S gene [see Fig. 5a1, and compare with Fig. 5a2,a3; also see Supplementary information 2 and 4 (slide No. 6)]. Clearly, the organization of rRNA genes can be complex when both 35S and 5S rRNA genes are co-localized53. The organizational complexity of overlapping 35S and 5S rRNA genes can be demonstrated by extended DNA fiber FISH71 and/or molecular methods72. In addition, sequencing information might show the details of joint organization of these genes47.
Ribosomal DNA signal variation
Homologous differences in rDNA signal intensities attributed to variation in rRNA gene copy number has been reported in several plant species48,58,59. In this study, while the 35S rDNA signal intensity for the mj-35S locus was about the same for both homologues of AC, it varied among the four NAAs of Chinese chestnut. Most striking was the large variation of signal intensity of the 35S rRNA gene between the homologues of CC3, suggesting dramatically different copy numbers. Dimorphic signal intensity in each of the mn-35S and 5S rDNA loci in AC and all four NAAs CC indicated copy number variation for these loci as well. Variation in copy numbers can result from unequal crossing over leading to higher copy numbers on one homologue relative to the other and may ultimately change the physical length of a locus, such as that observed for the NOR in other plant species [64,73; also observed in maize and ash, Islam-Faridi (unpublished)].
Chromatin composition and structural organization of satellites
The DAPI stain intensity proportionally reflects the AT to GC enrichment of underlying genomic regions, where less intense DAPI staining (pale/weak blue) under blue/UV filter is associated with euchromatin and more intense DAPI staining (bright/strong blue) is associated with heterochromatin34,74. Variations in intensity of staining allow clear differentiation of chromatin composition in early stages of the cell cycle, such as interphase and occasionally in late prophase and early pro-metaphase. The proximal region of the NOR-associated satellites of CC2 (see Fig. 2f), CC3 (see Fig. 5a) and CC4 (see Fig. 4f) may be euchromatic since these regions stained less intensely with DAPI. This may also be true for CC1 because the 35S FISH signal also appears in the proximal region of the satellite (see Fig. 2a). In addition, the 35S rDNA probe hybridized in these regions as was demonstrated through image analysis enhancement. This hybridization revealed that the rRNA genes were present in the proximal region of the satellites and not in the heterochromatic region. As shown on Figs. 5a and 7, a clear demarcation boundary separates these regions [also see Supplementary information 2 and 3 (PPT file and narratives, respectively), and 4 (PPT audio-video), slide Nos. 5 and 6]. Moreover, the interphase nuclei of CC3 (see Fig. 5b) and CC4 (see Fig. 5c) explicitly showed that there was no association of rRNA genes with the distal heterochromatic DNA of the individual satellites.
The distal region of the Chinese chestnut NOR-associated satellite is heterochromatic as shown by the intense DAPI stain while the proximal region may be euchromatic as it stained less intensely. The AC satellite also exhibited a weak DAPI stain indicating it may be entirely euchromatic. This analysis was possible due to the increased resolution obtained in interphase and in the early stages of the mitotic cell cycle. Once the chromosomes reached their maximum or near-maximum condensation in metaphase (and sometimes in pro-metaphases), we could not differentiate the chromatin composition in the satellites. Garcia et al.47 reported that 2949 karyotypes of 1791 plant species had been developed based on metaphase FISH, and earlier Zoldoz et al.59 reported that the NOR-associated satellites were heterochromatic. It is unlikely FISH image analysis in these studies was carried out on the early stages of the cell cycle such that the details of the rDNA and chromatin organization could be determined. Additional research conducted in the early stages of mitosis of various plant species should shed light on whether the rRNA gene(s) resides in euchromatin of the NOR-associated satellites.
While the secondary constriction (SC) is traditionally viewed as the NOR site, using a 35S rDNA probe in CC we observed that the NOR spans the end of the short arm, the SC and the proximal portion of the satellite. For AC, the NOR occupies the end of the short arm, the SC and the entire satellite. A similar distribution of a mj-35S rDNA signal was observed in Baobab (Adansonia digitata L.)55 and ash species (Fraxinus spp.)53. Further, we observed that the SC did not stain with DAPI (i.e., DAPI negative) (see Fig. 7b4,b8). Three consecutive A-T base pairs are required to bind with DAPI75. This suggests that such arrangements are absent in this region. It has been reported that the mj-35S sites showed no stain with DAPI, but stained brightly with CMA3, indicating they are GC-rich48,59. In fact, it is the secondary constriction that is DAPI negative, not the complete 35S site. Most FISH data were based primarily on condensed metaphases, so the structural details of the NOR were missing.
We observed no differences in the satellites associated with the NOR between the homologues in CC1 and CC2, but the homologues differed in CC3 and CC4 (see Supplementary Fig. S1B). Because of natural outcrossing and inter-species hybridization in Castanea, the pollen parents of the CC3 and CC4 NAA seedlings might be a species other than C. mollissima. However, for CC1 and CC2 the pollen parents were most likely to be C. mollissima since the homologous pair of each satellite showed similar cytological features. For CC3, one homologue’s satellite was composed of only a small body of chromatin like AC that stained less intensely with DAPI, suggesting that this satellite entirely lost its heterochromatic portion. This homologue might have been pre-existent in the ancestral background of CC3, or it could be contributed either by C. crenata or C. sativa as discussed earlier. For CC4, the heterochromatic region of one homologue’s satellite was smaller than the other (see Fig. 4e,f; Supplementary Fig. S1Bc1–3), which suggests the smaller satellite (SAT-2) lost a noticeable portion of heterochromatic DNA. The SAT-2 bearing chromosome might have been contributed by C. pumila, (chinquapin, a sister clade to the chestnuts), as they are common in the area where CC4 was derived and are known to hybridize with chestnuts76. Additional research is needed to confirm this hypothesis. For example, if the smaller satellite of CC4 was consistent with that found in C. pumila then our findings of chromatin composition in the NOR-associated satellite would be supported. Further, the SAT-1 of the NAAs CC that we studied were observed to be similar in physical size and chromatin composition. Regardless of the source of the NOR-associated satellite, the proximal region was stained less intensely with DAPI and hybridized with 35S rDNA composed of euchromatin. Additional research conducted in the early stages of mitosis should shed light on whether the rRNA gene(s) resides in the weakly stained chromatin of the NOR-associated satellites.
GISH of the F1 hybrid between Chinese and American chestnuts failed to differentiate the chromosomes of the two parental species. Cross-hybridization was observed in both genomes among all chromosomes (see Fig. 7a) showing the lack of significant differences in repetitive DNAs (see review by Schubert et al.57). Nevertheless, the presence of the distal segment of the large satellite extending beyond the 35S signal in the NOR bearing chromosome of Chinese chestnut enabled us to discriminate between Chinese and American chestnuts for this region of the genome. We observed the large satellite on the NOR bearing chromosomes in all four NAAs of Chinese chestnut was on just a single chromosome in the F1 hybrid. In addition, when Chinese chestnut DNA was used as a labeled probe, the satellite exhibited a strong bright green signal under a FITC filter (see Fig. 7b2) and intense blue signal under a DAPI filter (see Fig. 7b4, arrow). This suggests that this distal region is AT-rich and thus highly heterochromatic34,74. This area remains condensed throughout the cell-cycle, except when it replicates in late S-phase77. It is worthy to note that this region might be species and/or chromosome specific39,78,79. The molecular methods of cloning followed by FISH could confirm this notion. Heterochromatin is typically gene-poor and transcriptionally silent compared to euchromatin, and it was thought to serve as a graveyard for selfish mobile DNAs. However, recent studies suggest otherwise, i.e., heterochromatin contributes to important roles in cellular functions, such as transcriptions, chromosome segregation and long-range chromatin interactions (see reviews by Grewal and Jia80; Tamaru81). Currently, the biological significance of the heterochromatic DNA in the Chinese chestnut satellite is unclear. DNA sequence data for this satellite should begin to provide some information as to its significance and possible role in differentiating the species. In addition, a comparative study involving an AC SAT in CC cytoplasm and vise-versa should shed light on any interaction in a different genetic background.
Summary and conclusions
We characterized the organization and distribution of the ribosomal RNA genes (35S rDNA and 5S rDNA), and the structural and chromatin composition of the NOR-associated satellites in American and Chinese chestnuts. Two 35S rDNA loci (one major and one minor) and one 5S rDNA locus were identified in each species. We also identified a second 5S rDNA site linked distally to the major 35S rDNA locus in two of the four unrelated North American accessions of Chinese chestnut. Based on prophase and pro-metaphase FISH, we demonstrate that in both species the minor 35S and 5S loci were located proximally near the centromeric region in two non-homologous, near-metacentric chromosomes. The major 35S rDNA was in terminal and sub-terminal positions in American and Chinese chestnuts, respectively. The satellite of Chinese chestnut may be determined to be composed of euchromatic and heterochromatic regions of DNA while the American chestnut satellite may be composed of euchromatin. Immunostaining of histone markers will validate the chromatin composition within the satellites. This endeavor will be integrated into our next phase of cytogenomic research. In Chinese chestnut, we found that the distal segment of the major 35S gene, with or without the second 5S, was exclusively located in the proximal region of the satellite. This is the first instance, to our knowledge, that a plant species’ satellite has been identified to have unique chromatic regions of DNA. To clearly demonstrate and summarize these findings, we have prepared a fully animated and automated PowerPoint presentation that includes narratives, and an audio-video component (see Supplementary information 2, 3 and 4, respectively).
Further research using rDNA in FISH in early stages of the cell cycle and image analysis in different plant species should shed light on the chromatin composition in the NOR-associated satellites, and whether the ribosomal gene integration with the euchromatin in the NOR-associated satellite is a common feature.
Since the American and Chinese chestnut genomes have been sequenced, the use of molecular cytology (e.g., oligo-FISH) should further broaden our understanding of the structure and organization of the individual chromosomes of the Castanea species. Oligo-FISH probes will be used in future research to continue the study of the structural organization of the genome. In addition, a comparative FISH study of the DNA composition of the species’ major 35S rDNA bearing chromosome using genetically mapped probes should reveal the genomic and genic differences that could be essential to optimize interspecies backcross breeding strategies for the incorporation of disease resistance into American chestnut.
Materials and methods
Plant materials
Open-pollinated seeds were collected from two Chinese chestnut trees (Veselicky, in Pittsburgh PA and Don Surrette, in Pisgah, NC), two Chinese chestnut cultivars (‘AU-Cropper’ and ‘Qing’, in an orchard at the University of Missouri, Columbia, MO), and one American chestnut tree (provided by Dr. Thomas Kubisiak, Southern Institute of Forest Genetics, Saucier, MS). Control-pollinated F1 hybrid seeds (Chinese × American) were provided by Mr. William White of The American Chestnut Foundation, Meadowview, VA. Seeds were germinated and grown in potting mix (MetroMix SunGrow SB-650, Sun Gro Horticulture, Agawam, MA, USA) in a greenhouse in College Station, TX. In this study we refer to these Chinese chestnut trees (parents and their progeny) as North American accessions (NAAs) of Chinese chestnut (or NAAs CC), and specifically Veselicky as CC1, Don Surrette as CC2, ‘AU-Cropper’ as CC3, and ‘Qing’ as CC4. The American chestnut and F1 hybrid progeny are referred to as AC and F1, respectively. All parental Chinese chestnut trees utilized in this research have been established in the United States for decades through public breeding programs of USDA-ARS Beltsville, MD, Connecticut Agricultural Experiment Station, University of Missouri or the American Chestnut Foundation. These trees and samples of their progeny have been used by publicly supported researchers over these decades and are considered part of the public domain. This research was conducted in full compliance with IUCN Policy Statement on Research Involving Species at Risk of Extinction and the Convention on the Trade in Endangered Species of Wild Fauna and Flora. For example, only non-lethal samples were utilized, no samples were collected in the wild, and no plants or samples were moved across international boundaries.
Slide preparation for FISH
To accumulate metaphase chromosomes, actively growing root tips, about 1 cm long and with a milky white transparent appearance, were placed in the dark in an aqueous solution saturated with 0.8% of α-bromonaphthalene for 2 h or a solution of 2.5 mM hydroxyquinoline for 3.5 h followed by fixation in 4:1 (95% ethanol:glacial acetic acid). Fixed root tips were enzymatically processed to prepare chromosome spreads using a modification of the procedure of Jewell and Islam-Faridi82. The enzyme solution consisted of 40% (v/v) Cellulase (C2730, Sigma-Aldrich, St. Louis, MO, USA), 20% (v/v) Pectinase (P2611, Sigma-Aldrich), 2% (w/v) Cellulase RS (SERVA Electrophoresis GmbH, Heidelberg, Germany), 3% (w/v) Cellulase R10 (Yakult Pharmaceutical, Ind. CO., Tokyo, Japan), 1% (w/v) Macerozyme (Yakult Pharmaceutical, Ind. CO., Tokyo, Japan), and 1.5% (w/v) Pectolyase Y23 (Kyowa Chemical Products, CO., Osaka, Japan) in a 0.01 M Citrate buffer (pH 4.5). Digested root tips were washed four times with the same buffer and then macerated on ethanol (95%) cleaned glass slides (1 root per slide) in a drop of 3:1 (ethanol:glacial acetic acid). Chromosome spreads of individual seedlings were prepared as described elsewhere82.
Azure-B stain
The chromosome spreads were stained with 1% Azure-B (A4043, Sigma, St. Louis, MO) in 0.01 M Phosphate buffer pH (7.0) for 4 min at RT followed by a rinse in ddH2O. The slides were then dried overnight in a 37 C incubator. The preparation was made permanent with a drop of Permount (SP15, Fisher Scientific, Fair Lawn, NJ) under a glass cover-slip (22 × 40 mm). Chromosome spreads were viewed in bright field microscopy (AxioImager M2, Carl Zeiss, Göttingen, Germany) with a 63× plan apo-chromatic objective. Digital images were recorded under a green filter. The resolution of the captured images was increased to 300 dpi from 72, converted to black and white, and processed using Adobe Photoshop (Adobe Systems Inc., Broadway, NY).
Fluorescence in situ hybridization
Three cloned DNAs were used as fluorescent in situ hybridization (FISH) probes: 18S–5.8S–26S rDNA of maize83, 5S rDNA of sugar beet including the spacer region84, and Arabidopsis-type telomere repeat sequence (TTTAGGG)n (ATRS) (kindly provided by Dr. T. McKnight, Department of Biology, Texas A&M University). The probes were labeled with biotin-16-dUTP (Biotin-Nick Translation Mix, Roche, Mannheim, Germany) and/or digoxigenin-11-dUTP (Dig-Nick-Translation Mix, Roche, Mannheim, Germany) using the manufacturer’s instructions. Agarose gel electrophoresis was used to check the fragment sizes of the probe DNA and labeled nucleotide incorporation was verified by dot-blotting. For genomic in situ hybridization (GISH), genomic DNA of the Chinese chestnut tree ‘HHR3T1’ was labeled with digoxigenin-11-dUTP as described elsewhere85.
Standard FISH or GISH techniques were utilized as reported previously54,85. Hybridization sites of biotin-labeled and digoxigenin-labeled probes were detected using Cy3-conjugated streptavidin (Jackson ImmunoResearch Laboratories, West Grove, PA, USA) and fluorescein-conjugated sheep anti-digoxigenin (Roche, Mannheim, Germany), respectively. Slides were counter-stained with DAPI (4 μg/ml) in McIlvaine buffer, pH 7.0 (9 mM citric acid, 80 mM Na2HPO4, 2.5 mM MgCl2), and a small drop (~ 10 μl) of Vectashield (Vector Laboratories, Burlingame CA, USA) was added to prevent photo-bleaching of the fluorochromes. Three FISH experiments and one GISH experiment were conducted as specified below.
FISH: Experiment 1: American chestnut (AC) and Chinese chestnut (CC1) chromosome spreads were probed with 35S and 5S rDNAs. Experiment 2: The ATRS probe was used along with the 35S rDNA (as a control) on the AC chromosome spreads to investigate the terminus of the major 35S rDNA bearing chromosome, since it was completely covered by 35S signal. Experiment 3: Three additional NAAs of Chinese chestnut (CC2, CC3 and CC4) were probed with 35S and 5S rDNAs.
GISH: Since the NOR-associated satellite was heterochromatic in the NAAs CC but not in AC, we used GISH of an F1 hybrid to provide a common background with 35S rDNA and DAPI staining to characterize the differences in the satellites’ structural organization and chromatin composition. Total genomic DNA from Chinese chestnut (DNA of the tree ‘HHR3T1’, a ramet of cv ‘Kuling’ provided by Dr. T. Kubisiak, Southern Institute of Forest Genetics, Saucier, MS) was used as a probe while total genomic DNA from American chestnut (DNA of the tree ‘GMBig’ also provided by Dr. T. Kubisiak) was used as blocking DNA to differentiate Chinese and American chestnut genomes in the F1 hybrid.
Digital image capture and process
Fluorescent in situ hybridization images of chromosome spreads were viewed using a 63× plan apochromatic objective or a 100× plan-neofluor objective on an epi-fluorescence microscope (AxioImager M2, Carl Zeiss Inc., Göttingen, Germany) fitted with suitable filter sets (Chroma Technology Corp., Bellows Falls, VT, USA). Digital images were captured and recorded with a Cool Cube 1 high performance charge-coupled device (CCD) camera (MetaSystems Group Inc., Boston, MA, USA). Images were pre-processed with ISIS v5.1 (MetaSystems Group Inc., Boston, MA USA) and further processed with Adobe Photoshop CC2019 (Adobe Inc., San Jose, CA USA) after increasing the resolution from 72 to 300 dpi.
Data availability
All data generated and analyzed for this study are included in this article as well as its Supplementary Document files.
Change history
27 May 2024
A Correction to this paper has been published: https://doi.org/10.1038/s41598-024-62279-6
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Acknowledgements
We thank Dr. M. Majid for his assistance in caring for the chestnut seedlings in the greenhouse and helping with cytology work. Also, we extend our thanks to Drs. Hamidou Sakhanokho and Barbara Smith (USDA-ARS, Poplarville, MS, USA), Bir Singh (Texas A&M University, College Station, TX, USA) for their critical reading and valuable comments on the manuscript. We appreciate Dr. Fred. Raley (Texas A&M Forest Service) for providing valuable comments and allowing us to use the greenhouse facilities. We are also grateful to the Texas A&M IT support staff (Ms. J. Gould, Mr. R. McAllister and Mr. S. Vajdak) for their assistance with the PowerPoint audio.
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The use of trade, firm, or corporation names in this publication (or page) is for the information and convenience of the reader. Such use does not constitute an official endorsement or approval by the United States Department of Agriculture, the Forest Service of any product or service to the exclusion of others that may be suitable.
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N.I-F. conceived and performed experiments (chromosome spreads, FISH and image analysis), N.I-F. and G.H. wrote the manuscript; C.D.N. revised the manuscript; T.Z., L.G., F.H., P.S. and C.D.N. provided technical and editorial comments; P.S. arranged for and/or collected the seeds and seedlings for the research. All authors reviewed and approved the manuscript.
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Islam-Faridi, N., Hodnett, G.L., Zhebentyayeva, T. et al. Cyto-molecular characterization of rDNA and chromatin composition in the NOR-associated satellite in Chestnut (Castanea spp.). Sci Rep 14, 980 (2024). https://doi.org/10.1038/s41598-023-45879-6
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DOI: https://doi.org/10.1038/s41598-023-45879-6
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