Abstract
The curiosity to discover transcription factors to reprogram somatic cells to induced pluripotent stem cells (iPSCs) resulted in the identification of a reprogramming factor, Gli-similar transcription factor GLIS1. This proline-rich Kruppel-like zinc finger transcription factor has a role in embryonic development, iPSC generation, and cancer. The spatial and temporal expression of GLIS1 during embryonic development implicates that it can control gene expression at specific developmental stages. Moreover, GLIS1 in combination with OCT4, SOX2, and KLF4 reprogramming factors resulted in an increase in reprogramming efficiency, giving rise to primarily bona fide iPSCs. Mutations in the GLIS1 gene are associated with several types of tumors and cancers, and it shows a tissue-specific function where it acts either as an oncogene or as a tumor suppressor gene. This review gives a comprehensive overview of GLIS1 and its important role in embryonic development, cancer, and the generation of iPSCs.
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Keywords
- Cancer
- Cell reprogramming
- Embryonic development
- GLIS1
- Induced pluripotent stem cells
- Transcription factor
1 Introduction
Stem cells and their role in regenerative medicine are a developing field in biomedical science. Understanding the mechanisms involved in stem cell self-renewal and differentiation holds great importance in unraveling the potential and their subsequent use in various biomedical applications. Fundamentally, they are undifferentiated cells that have the potential to self-renew and differentiate and are classified into different stem cell types such as embryonic stem cells (ESCs), fetal stem cells, and adult stem cells (Roobrouck et al. 2008). ESCs are pluripotent cells that can be differentiated into cells of all three germ layers, namely ectoderm, endoderm, and mesoderm (Poh et al. 2014), thereby having immense utility in disease modeling and other biomedical applications. The ethical limitations associated with the use of ESCs restrict their use in patient-specific applications. To overcome this limitation and generate pluripotent stem cells in a laboratory, Yamanaka and group found that using a combination of OCT4, SOX2, KLF4, and c-MYC (OSKM) transcription factors, mouse and human fibroblasts can be reprogrammed to an early embryonic stem cell-like state, which they termed as induced pluripotent stem cells (iPSCs) (Takahashi et al. 2007; Takahashi and Yamanaka 2006). In the subsequent year, Thomson and group also independently generated iPSCs using the factors OCT4, SOX2, LIN28A, and NANOG, which were capable of reprogramming human somatic cells to iPSCs (Yu et al. 2007). These two findings revolutionized the field of regenerative medicine and since then, multiple transcription factors have been screened for elucidating their roles in enhancing or substituting OSKM reprogramming transcription factors for the generation of mature iPSCs (Dey et al. 2021a, b, c; Raina et al. 2021; Thool et al. 2022a). The caveat of using OSKM for the generation of clinical-grade iPSCs was the formation of a heterogeneous population of iPSC colonies comprising fully reprogrammed cells (bona fide iPSCs; rarely) and incompletely reprogrammed cells (transformed colonies; mostly) (Maekawa et al. 2011). Also, the presence of c-MYC makes OSKM-based reprogramming less worthy for clinical applications due to its tumorigenic potential (Akifuji et al. 2021). Gli-similar 1 (GLIS1) is one of the factors that was reported to enhance the formation of fully mature iPSC colonies when included with OSK (Maekawa et al. 2011).
GLIS1 gene was identified independently by two groups based on sequence homology to Gli zinc finger domain (Kim et al. 2002; Nakashima et al. 2002). It belongs to the family of Kruppel-like zinc finger transcription factor, which is one of the largest family of transcription factors that work as activators and repressors of gene transcription (Kim et al. 2002). Moreover, GLIS1 is found to be expressed during early embryonic development and has a critical role in the control of gene expression during specific stages of embryonic development (Kim et al. 2002). These attributes made GLIS1 to be quoted as “the fifth Yamanaka factor” in reprogramming. In addition, high expression of GLIS1 is also found to be associated with different tumors and cancers (Kim et al. 2022; Shimamoto et al. 2020; Vadnais et al. 2014). In this review, a detailed discussion on the importance of GLIS1 in embryonic development, cancer, and iPSC generation is reported.
2 GLIS1 Gene
GLIS1 is a protein-coding gene (Table 1) that acts as both an activator and repressor of transcription (Kim et al. 2002). It is localized on chromosome 1 at 1p32.3 in humans and chromosome 4 at 4C6 position in mice (Kim et al. 2002). The gene is conserved in chimpanzees, rhesus monkeys, dogs, cows, mice, rats, chickens, and zebrafish, with 250 organisms having orthologs with the human GLIS1 gene (Yasuoka et al. 2020). It is also reported that GLIS1 has paralogs such as GLIS3, GLI2, GLI3, GLIS2, GLI1, ZIC5, ZIC2, ZXDC, ZIC3, ZIC1, ZXDB, ZXDA, AEBP2, and ZIC4.
3 GLIS1 Protein
Human GLIS1 protein is 620 amino acids in length (Fig. 1) having a molecular weight of ~66 kDa, while mouse GLIS1 protein consists of 789 amino acids with a molecular weight of ~84 kDa (Lee et al. 2017). It belongs to the GLIS subfamily of Kruppel-like zinc finger transcription factors, which is the largest family of transcription factors (Kim et al. 2002; Scoville et al. 2017). It is closely related to GLI and ZIC subfamilies with GLIS2 and GLIS3 as other protein members of the same family (Scoville et al. 2017). GLIS1 is a neutral protein with a theoretical pI of 7.56. It is also a proline-rich protein with 12.4% proline content. The sequence identity between human and mouse GLIS1 proteins is 83.2%. Furthermore, on analyzing the protein sequence using the InterPro database, the zinc finger domain was found to have five Cys2-His2-type zinc finger motifs with the consensus Cys-X4-Cys-X12,15-His-X3,4-His belonging to GLI Cys2-His2-type zinc-finger protein family (Fig. 1). InterPro scan and profile scan analysis also identified a potential bipartite nuclear localization signal between Arg511 and Lys527 that overlaps with the fifth zinc finger motif of GLIS1. The region containing the zinc finger domain and bipartite nuclear localization signal was important for the nuclear localization of GLIS1. It has a strong activation domain at the C-terminal end that can mediate its interaction with a co-activator, thus functioning primarily as a transcriptional activator (Jetten et al. 2022; Kim et al. 2002). The main co-activator of GLIS1 is EP300/p300, which is recruited to the transactivation domain present at the C-terminal end (Jetten et al. 2022). It also contains a repressor domain in its N-terminal end that functions as a transcriptional repressor (Jetten et al. 2022). The highly conserved DNA-binding domain (zinc finger domains) has five tandem repeats of Cys2-His2 zinc finger motifs. These motifs bind to the GLIS binding sites, which are oligonucleotides containing G-rich consensus sequence ((A/G) GG(G/A) GG) (Scoville et al. 2017). In general, this protein acts as an activator or repressor of gene transcription as it contains both transactivation and repressor domains (Kim et al. 2002).
The three-dimensional crystal structure of GLIS1 protein is not reported to date. The 3D structure of the protein was obtained from the Alphafold database (Fig. 2a). The secondary structure of the protein was predicted using the online bioinformatics tools GOR4, SOPMA, and PSIPRED (Fig. 2b). Using these tools, the predicted structure reveals that GLIS1 mainly consists of random coils (77%) (Fig. 2b). The amount of α-helices is around 17% and β-sheets is around 6% (Fig. 2b). Random coils or intrinsically disordered regions are a characteristic feature of transcription factors, which is necessary for its functionality (Garza et al. 2009). The amino acid composition of GLIS1 protein reveals that it contains more proline (12.4%), serine (11%), and leucine (11%) residues that might contribute to the transactivation activity of GLIS1 (Chin et al. 1997).
The interacting partners of GLIS1 protein were analyzed using the STRINGv11 database as depicted in Fig. 3. The suppressor of fused homolog protein, which is a negative regulator of Hedgehog signaling pathway (Takenaka 2007), regulates developmental processes in multicellular embryos and is found to be a direct interacting partner of GLIS1 and other GLI family proteins GLI1, GLI2, and GLI3. NR2C1, an interacting partner of GLIS1, is also reported to activate OCT4 gene expression and forms the core of direct repeat erythroid-definitive complex that represses the transcription of embryonic and fetal β-globin (Park et al. 2007; Tanabe 2002; Tanabe et al. 2007). GLIS1 also interacts with MYCL, which is a proto-oncogene belonging to the MYC family, thereby having the potential to replace c-MYC in OKSM-based reprogramming (Schwab 2004). Furthermore, CAMK4 is a direct interacting partner of GLIS1, which regulates the activity of transcriptional activators such as CREB1, MEF2D, JUN, and RORA by phosphorylation. This plays important roles in immune response, inflammation, and memory consolidation (Naz et al. 2020). Also, GLIS1 was found to have three potential CAMK4 phosphorylation sites at Ser72, Ser187, and Thr458 (Kim et al. 2002). It was reported that CAMK4 can enhance the transcriptional activation mediated by GLIS1 fourfold (Kim et al. 2002). Interestingly, an association of GLIS1 with KLK4 was reported, which might be an indication of the involvement of GLIS1 in the pathogenesis of Parkinson’s disease, since KLK4 has roles in degrading α-synuclein and preventing its aggregation (Song et al. 2012; Sotiropoulou et al. 2009). These experimental evidence indicate the association of GLIS1 in various physiological functions.
4 Role of GLIS1 in Embryonic Development
The expression of GLIS1 was first observed during early stages of embryonic development in mice (Kim et al. 2002). Predominant expression of GLIS1 was observed in unfertilized oocytes and one-cell stage murine embryo followed by a moderate expression in the two-cell stage and lowest at the four-cell stage (Fig. 4) (Jetten 2018; Nakashima et al. 2002). The expression was absent or observed in trace amounts in the eight-cell stage; however, no expression was observed in the subsequent stages (16-cell stage, morula and blastocyst) (Fig. 4) (Nakashima et al. 2002). Also, transient expression of GLIS1 was observed in several defined structures of mesodermal lineage, including craniofacial regions, follicles, branchial arches, limb buds, somites and myotomes, genital tubercle, and tailbud during embryonic development (Kim et al. 2002). Its expression was detected in extraembryonic tissues and lateral mesoderm during gastrulation in mice (Kim et al. 2002). It is expressed both spatially and temporally during embryonic development, implying that it can regulate several steps in organogenesis (Kim et al. 2002). GLIS1 protein showed a low level of expression in mouse embryonic stem cells (ESCs) and its overexpression led to reduced proliferation of ESCs (Maekawa et al. 2011; Wang et al. 2019). Moreover, GLIS1 protein plays a crucial role in controlling gene expression during specific stages of embryonic development (Kim et al. 2002).
GLIS1 plays a regulatory role during heart development and is expressed predominantly in the nuclei of endothelial and interstitial cells of mitral valves in mice during embryonic development (Yu et al. 2019). It was retained in a subset of interstitial and endocardial cells during fetal gestation. The expression became much weaker during 6 months of age, with weaker expression detected in the myocytes, epicardium, and endocardium of the ventricular myocardium. This suggests that GLIS1 is embryonically regulated and likely to be involved in the regulation of valve morphogenesis during early development (Yu et al. 2019). Furthermore, it was reported that in adult mouse tissues, GLIS1 mRNA is highly expressed in the placenta and kidney, whereas its expression is low in testes, brain, colon, brown fat tissue, and thymus (Nakashima et al. 2002).
Downregulation of GLIS1 in bovine embryos led to failed zygotic genome activation, causing developmental arrest at the 16-cell stage (Takahashi et al. 2015). Studies reported that pyruvate dehydrogenase 1α and heat shock cognate protein 70 (HSPA8) gene expression was downregulated upon the silencing of GLIS1 gene (Takahashi et al. 2015). Pyruvate dehydrogenase 1α helps in murine and bovine embryo development and also in glucose metabolism. HSPA8 codes for heat shock cognate protein 70, which acts as a housekeeping and chaperone protein. This showed the critical importance of GLIS1 in the development of bovine oocytes and embryos (Takahashi et al. 2015).
In humans, GLIS1 is highly expressed in unfertilized eggs and one-cell embryos while it is very low in adult tissues (Fig. 4) (Jetten et al. 2022; Maekawa and Yamanaka 2011; Nakashima et al. 2002). A modest level of expression was seen in two-cell embryos and placenta (Jetten 2018; Nakashima et al. 2002). GLIS1 was most abundantly expressed in the kidney, with moderate expression in various other organs such as brain, thymus, adipose tissue, colon, testis, and placenta (Jetten 2018; Nakashima et al. 2002). The role of GLIS1 in human embryo development remains elusive and requires further investigation.
5 Role of GLIS1 in Cancer
GLIS1 belongs to the Glis subfamily of Kruppel-like transcription factors, which are closely related to the GLI family transcription factors that are part of the Hedgehog signaling pathway (Kim et al. 2003). These transcription factors are involved in the initiation and regulation of multiple oncogenic signaling pathways (Didiasova et al. 2018). Furthermore, the GLI genes, GLI2 and GLI3, were found to be highly associated with human cancers (Dahmane et al. 1997; Sheng et al. 2002). These transcription factors play a pivotal role in regulating biological processes, which are critical during oncogenesis such as stem cell renewal, differentiation, inflammatory responses, epithelial–mesenchymal transition (EMT), and cell proliferation by regulating gene expression (Dahmane et al. 1997; Sheng et al. 2002). Previous studies reported that GLIS1 protein was associated with several cancers such as breast cancer, colorectal cancer, thyroid tumor, ovarian cancer, hepatocellular carcinoma, and leukemia (Jetten et al. 2022).
GLIS1 was reported to be highly expressed in tumors with elevated Wnt gene expression (Vadnais et al. 2014). Interestingly, GLIS1 was found to act as an oncogene in breast cancer through its cooperation with Cux1 as it activated Wnt genes in human breast cancer cells via autocrine activation of Wnt/β-catenin pathway (Fig. 5a) (Vadnais et al. 2014). The elevated Wnt expression can be associated with high levels of GLIS1 along with the factor Cux1, which led to EMT (Vadnais et al. 2014). GLIS1 stimulates T cell factor or β-catenin transcriptional activity and helps in increasing cell migration and invasion (Vadnais et al. 2014). Moreover, high expression of GLIS1 in mammary tumor cells led to the activation of several Wnt genes by increasing expression of Wnt ligands such as Wnt3, Wnt4, Wnt5b, Wnt6, Wnt9a, Wnt10a, and Wnt10b in MCF10A cells (Fig. 5a) (Vadnais et al. 2014). It is known that higher expression of Wnt ligands is associated with autocrine activation of Wnt/β-catenin pathway that is seen in different cancers, especially breast tumors (Vadnais et al. 2014). When both GLIS1 and CUX1 were co-expressed, the highest expression of the Wnt expression was observed, along with an increase in the migration and invasion rate in mammary epithelial cells and enhanced mesenchymal–epithelial transition (MET) (Vadnais et al. 2014). Furthermore, in colorectal cancer, difference in hypermethylation of GLIS1 gene was seen along with four other genes involved in Wnt signaling without adenomatous polyposis coli mutation, suggesting a cancer formation mechanism in these tumors (Xicola et al. 2018). In contrary to its weak expression in adult tissues, high expression of GLIS1 was observed in cancers (Vadnais et al. 2014; Xicola et al. 2018).
GLIS1 is expressed in breast cancer tissues and is an important downstream target gene of microRNA 1-3p, which is a small noncoding RNA that regulates mRNA posttranscriptionally (Tao et al. 2021). Repression of GLIS1 by microRNA 1-3p by binding to 3′ untranslated regions led to impairment in progression and metastasis of breast cancer cells (Fig. 5b) (Tao et al. 2021). This indicates that GLIS1 downregulation has antitumor and antimetastatic functions. GLIS1 silencing in breast cancer led to a decline in cell migration and invasion along with the blocking of EMT (Fig. 5b) (Tao et al. 2021).
Previous studies reported GLIS1 as an important gene in the metastasis process (Kim et al. 2022). In a study to identify cancer-associated fibroblast (CAF)-related genes that regulate progression and metastasis in the tumor microenvironment in ovarian serous carcinoma, it was identified that GLIS1 expression level increased both mRNA and protein levels in metastatic cancer-associated fibroblasts (CAFs). It was shown that GLIS1 overexpression facilitated migration, invasion, and wound healing along with peritoneal metastasis in ovarian cancer cells (Fig. 6) (Kim et al. 2022). Moreover, metastasis of ovarian cancer can be inhibited by targeting GLIS1 in CAFs, thus making this a potent therapeutic target. On silencing GLIS1, properties such as motility, adhesion, angiogenesis, and metastasis of ovarian cancer cells were reduced both in vitro and in vivo (Fig. 6) (Kim et al. 2022).
Significantly, GLIS1 is evident in the regulation of several features that can be associated with malignancy such as EMT and risk of relapse (Chen et al. 2015). In high hyper diploid acute lymphoblastic leukemia (ALL) patients, it was identified that nucleotide variations downstream of GLIS1, which is a cell fate–determining transcription factor, created developmental disturbance. These variations led to increased risk of relapse in patients with high hyper-diploid ALL (Chen et al. 2015). Somatic mutations were also detected in GLIS1 along with other signaling molecules that were involved in B cell differentiation, proliferation, and cell death, and mutation in GLIS1 gene was deleterious in ALL cases (Chen et al. 2015).
Apart from these, GLIS1 was found to have a significant association with hyalinizing trabecular tumor (HTT), and therefore reclassifying HTT as “GLIS-rearranged hyalinizing trabecular adenoma” (Nikiforova et al. 2019). In this study, it was demonstrated that rearrangements of GLIS and PAX8 genes are a genetic hallmark of HTT. Gene fusions of GLIS1 or GLIS3 to PAX8 were formed by inter-chromosomal rearrangement, leading to overexpression of 3′ portion of GLIS genes containing intact DNA-binding zinc finger domain of these transcription factors (Nikiforova et al. 2019). Moreover, it was shown that GLIS fusion was highly specific in HTT, and also the malignant transformation is higher in tumors with GLIS1 fusion than GLIS3 fusion. This specificity and sensitivity of these fusions to HTT led to a remarkable improvement in the clinical management of patients, by detecting GLIS fusion in their samples by next-generation sequencing (Nikiforova et al. 2019). To pinpoint, GLIS fusion detection could be used in diagnosing HTT.
Furthermore, GLIS1 has promising roles in immunotherapy for hepatocellular carcinoma (Rong et al. 2023). In hepatocellular carcinoma, GLIS1 regulates the SGK-STAT3-PD1 pathway and promotes CD8+ T cell exhaustion. It was reported that the downregulation of GLIS1 led to a change in the infiltration ability of CD8+ T cells, blocked cancer development, and raised the anti-PD1 reaction of CD8+ T cells (Rong et al. 2023). Thus, GLIS1 can be a potential target for enabling anticancer immunity by the reversal of T cell exhaustion (Rong et al. 2023).
The current treatment strategies for cancer involves chemotherapy, radiotherapy, and surgery. An early diagnosis of cancer can help in a permanent cure, which is not available till now. Further exploration of the roles of GLIS1 in several cancers, and on using other biomarkers can detect cancer at an early stage, thus paving way to find a permanent cure.
6 Role of GLIS1 in iPSCs
The discovery of iPSCs revolutionized the field of regenerative medicine by unveiling a new research area in stem cell biology. The functional and molecular similarity of iPSCs to ESCs made them potential cell resources for disease modeling, drug discovery, toxicology screening, and autologous cell therapy (Thummer and Kaveeshwar 2023). Moreover, iPSCs can be used as a model to study tumorigenesis and drug resistance and early human development and as a promising tool for regenerative medicine (Ho et al. 2018; Thummer and Kaveeshwar 2023; Shi et al. 2017). Similar gene expression profiles of ESCs and iPSCs opened new frontiers to identify different pluripotency-associated genes, playing a role in embryonic development, helping overcome the ethical concerns associated with the use of embryos.
Human iPSCs were first generated by transducing OCT4, SOX2, KLF4, and c-MYC (OSKM) (Takahashi et al. 2007; Yu et al. 2007). The application of using human iPSCs in clinical therapies were restricted due to the presence of oncogenic factors such as c-MYC and KLF4 (Akifuji et al. 2021; Okita et al. 2007). To overcome this limitation and to generate human iPSCs, Maekawa and group evaluated a library of 1437 factors, out of which 18 factors including GLIS1 were found to have the ability to replace c-MYC by reprogramming human skin fibroblasts to iPSCs (Maekawa et al. 2011). In this study, the potential of GLIS1 in cellular reprogramming was highlighted as it markedly increased the number of iPSC colonies when co-introduced with OCT4, SOX2, and KLF4 (Fig. 7) (Maekawa et al. 2011). Furthermore, replacing c-MYC with GLIS1 increased the yield and efficiency of iPSC generation and prevented the generation of transformed colonies. Furthermore, it increased the reprogramming efficiency when synergistically expressed with c-MYC in both mouse and human dermal fibroblasts. Moreover, GLIS1 rescinds the tumorigenic effect by avoiding the potential genomic instability induced by c-MYC when co-expressed (Maekawa et al. 2011). To validate the efficacy of GLIS1 to generate iPSCs from human cancer cells, ovarian adenocarcinoma cells (PEO4) were reprogrammed using OKSG (Bindhya et al. 2021). Twofold increase and larger iPSC colonies were generated on replacing OSKM with OKSG. Notably, GLIS1 successfully replaced c-MYC in reprogramming ovarian cancer cell line and fallopian epithelial cells to iPSCs (Bindhya et al. 2021). A similar study reported the generation of iPSCs from newborn and adult human fibroblasts efficiently using OSKG (Yoshioka and Dowdy 2017). GLIS1 was found to be a successful candidate in the development of cancer model systems, where the elimination of oncogenic factors such as c-MYC is a prerequisite.
Similar reprogramming studies have shown the reprogramming of urine-derived cells to iPSCs using a combination of six factors OCT4, GLIS1, KLF4, SOX2, L-MYC, and miR-302, obviating the use of tumorigenic factors such as c-MYC, SV40-LT, and p53 inhibitor (Wang et al. 2017). Furthermore, the synergistic use of GLIS1 with OSKM cocktail increased the iPSC colonies significantly especially in old human fibroblasts and can be superior to a six-factor combination that includes LIN28A along with OSKMG and a four-factor combination using OSKM or OSKG (Yoshioka and Dowdy 2017). Similarly, an increase in iPSC colonies was seen in mouse fibroblasts when OSKMG cocktail was used for reprogramming (Yoshioka and Dowdy 2017). Notably, the chimeric mice that were generated from iPSCs induced using OKSG had longer survival times than those from OSKM (Maekawa et al. 2011). In human fibroblasts, similar colonies with better phenotype were obtained using OSKG and OSKMG than OSKM cocktail (Yoshioka and Dowdy 2017). In a quest to find other reprogramming cocktail, it was found that GLIS1 in combination with six factors (JDP2, JHDM1B, MKK6, GLIS1, NANOG, ESSRB, and SALL4) could reprogram mouse embryonic fibroblasts to iPSCs with high quality and efficiency, thus providing an alternative to Yamanaka factors for achieving pluripotency (Wang et al. 2019). These seven-factor colonies were easier to pick and passage to establish iPSC lines. Compared to OKSM factors, these seven-factor iPSC colonies containing GLIS1 are of high-grade ESC quality (Wang et al. 2019). Furthermore, these factors produced high-quality chimeras better than OSKM iPSCs, which support germline transmission and tetraploid complementation. GLIS1 was reported to function as a chromatin remodeler, thereby opening the chromatin structure to assist reprogramming (Wang et al. 2019). Other studies have also reported that iPSC lines can be developed from the fibroblast of cystic fibrosis (CF) patients with mutation in cystic fibrosis transmembrane conductance regulator (CFTR) gene by using GLIS1 along with OSKM factors for reprogramming (Kondrateva et al. 2021a, b). Two iPSC cell lines (RCMGi004-A and -B) were derived from human skin fibroblasts of CF patients with heterozygous mutation in CFTR gene when GLIS1 along with OKSM factors were used for reprogramming (Kondrateva et al. 2021b). These cell lines showed the potential to differentiate into all three germ layers and expressed all ectodermal, endodermal, and mesodermal markers (Kondrateva et al. 2021b). Another study also showed the derivation of iPSC cell line (RCMGi002-A) from dermal fibroblast of CF patients with a homozygous mutation in the CFTR gene. Both these cell lines can be used for disease modeling, drug screening, and genome editing for the personalized treatment of CF (Kondrateva et al. 2021a, b).
Besides iPSCs, the induced tissue-specific stem cells, which does not have the risk of teratoma formation can also be developed from mouse pancreatic tissues using OSKG factors, utilizing single synthetic self-replicative Venezuelan equine encephalitis reprogramming factor RNA replicon (Miyagi-Shiohira et al. 2018). Similarly, induced tissue–specific stem cells were generated from aged mesenchymal cells derived from adipose tissues by expressing OSKG factors. Furthermore, clonal human iPSC colonies were obtained on reprogramming urine-derived cells with OSKMG factors using self-replicative RNA as vector by obtaining a reprogramming efficiency of 0.008–0.17% in a single experiment (Miyagi-Shiohira et al. 2018).
GLIS1 functions as a strong promoter of somatic cell reprogramming by directly interacting with zinc finger domain of KLF4 via its N-terminal domain. It also induced the expression of the forkhead box, FOXA2, and several Wnt genes to enhance MET to promote reprogramming (Maekawa et al. 2011). FOXA2 is a transcription factor that antagonizes EMT, which is a prerequisite for iPSC colony formation. GLIS1 increased the expression of several genes such as ESRRB, WNT3, WNT6, WNT8A and WNT10A, LIN281, NANOG, MYCN, MYCL, TSPAN, NRGN, and FOXA2, which can also increase iPSC colony formation (Maekawa et al. 2011). MYCN and MYCL were regulated directly by GLIS1, whereas FOXA2, ESRRB1, and LIN28A transcription was regulated indirectly (Maekawa et al. 2011). GLIS1 also promoted multiple preprogramming pathways including Wnt signaling and regulated several genes involved in MET. It also induced multilevel epigenetic and metabolic remodeling in stem cells. During somatic cell reprogramming, GLIS1 indicated a unique multilevel path to pluripotency by initiating an epigenome-metabolome-epigenome cascade without affecting MET (Li et al. 2020). It led to the repression of somatic genes at the chromatin level. Also, it binds to pluripotent and glycolysis genes and opens them, which resulted in the activation of glycolysis and increase in lactate and acetyl-coenzyme A levels (Li et al. 2020). During acquiring pluripotency, glycolysis genes were key targets of GLIS1. Thus, GLIS1 bound to most glycolysis genes, activated their expression, and enhanced reprogramming by upregulating glycolytic activity (Li et al. 2020). It also increased histone acetylation and deacetylation on promoters of pluripotency genes (Li et al. 2020). Furthermore, the metabolites of glycolysis pathway and tricarboxylic acid cycle increased in the presence of GLIS1, and upon its overexpression, there was an increase in the levels of nucleotide-related molecules except adenosine triphosphate, increase in acetyl-coenzyme A levels, glucose uptake, and secretion of lactate. This study suggested that GLIS1 modulated histone acetylation and lactylation during somatic cell reprogramming by increasing their levels on promoters of pluripotency genes and activating their expression (Li et al. 2020). GLIS1 facilitates a complex sequential closed to open chromatin shift of glycolysis genes, leading to similar shift of pluripotent genes (Li et al. 2020). This study shed light to understand the function of GLIS1 during embryonic development and cancer with respect to the epigenome-metabolome-epigenome cascade mediated by it, as the level of glucose and pentose phosphate pathway metabolized are low in oocytes, and it increases on sperm entry, and cancer also relies on glycolysis to supply energy (Li et al. 2020). In total, 19,494 binding sites were identified for GLIS1 that displayed enrichment close to transcription start site and upstream regions of genes (Li et al. 2020). The genes involved in the glycolytic process such as Hk2, Pgk1, Pfkl, Pkm, Eno1, and Ldha were upregulated, and some of the genes involved in maintaining somatic state such as Setbp1, Thy1, Il1rn, Prss23, Col6a2, Col6a3, and Col1a1 were downregulated when GLIS1 was used for reprogramming (Li et al. 2020). There was a dual binding mechanism of GLIS1 to upregulated and downregulated gene targets that activated glycolytic process by increasing the expression level of associated genes and suppressing somatic state by inhibiting the gene expression (Li et al. 2020). Studies also identified that GLIS1 enables reprogramming of senescent cells (senescent mouse embryonic fibroblasts) into pluripotent cells and improves the genomic stability, suggesting that it can be used in regenerative medicine for elderly subjects (Li et al. 2020). Furthermore, it reduced p16 expression and alleviated senescent phenotype.
GLIS1 can be a better tool for iPSC technology as it generates completely reprogrammed cells by suppressing partially reprogrammed cells that still expresses GLIS1. Also, reprogramming by GLIS1 is independent of the cell type and method used (Li et al. 2020). Additionally, it specifically promoted iPSCs and not partially reprogrammed or transformed cells (Maekawa et al. 2011), primarily because it suppressed proliferation when expressed in cells that do not express it. GLIS1 had similar effects in reprogramming in both mice and humans. Moreover, on expressing GLIS1 with OSK factors in mouse fibroblasts, completely reprogrammed cells were produced, and iPSC colonies increased from 10% to 50% in human fibroblasts (Maekawa et al. 2011; Maekawa and Yamanaka 2011). More iPSCs were formed when OSKG factors were used, which were larger in size and tightly packed with defined borders compared to those derived from the OSKM combination (Maekawa et al. 2011). GLIS1 increased reprogramming twofold as compared to OSKM and 30-fold as compared to OKS factors, and therefore, it is recognized as an enhancer of reprogramming. It is a powerful reprogramming factor and is called the “fifth Yamanaka reprogramming factor,” thus having great clinical potential. (Li et al. 2020).
7 Conclusion and Future Perspectives
GLIS1 is a nuclear localized protein, which acts as an activator and repressor of gene transcription. It is expressed in unfertilized oocytes and one-cell embryo of both mice and humans. GLIS1 regulates different functions related to cell adhesion, proliferation, differentiation, extracellular matrix, and chemotaxis. Even though not much is known about the physiological functions of GLIS1 in adult tissues, it was found to be associated with different types of cancers and is still elusive in the cancer paradigm. The suppression of GLIS1 was reported to be associated with suppressed carcinoma, metastatic developments, and CD8+ T cell exhaustion (Tao et al. 2021; Shimamoto et al. 2020; Kim et al. 2022; Rong et al. 2023). Association of GLIS1 with Wnt and cell cycle pathways (Shimamoto et al. 2020) and its link with SGK1-STAT3-PD1 pathways in eliciting immune suppressive microenvironments and activation of immune cells, such as natural killer cells, dendritic cells, monocytes, and macrophages upon its downregulation (Rong et al. 2023), opens a plethora of avenues for potential research. Elucidating the role of GLIS1 in the regulation of exocellular vesicles and modulation of immune microenvironment and their role in tumor progression can help generate effective anticancer immunotherapies in near future. Besides cancer, a significant association between a GLIS1 variant and glaucoma was identified in humans (Nair et al. 2021). GLIS1 has an important role in regulating functions of trabecular meshwork whose dysfunction leads to chronically elevated intraocular pressure (Nair et al. 2021). This is a risk factor in glaucoma, which results in blindness. GLIS1 helps in maintaining the structure of trabecular meshwork, aqueous humor dynamics, and normal intraocular pressure, and therefore it was identified as a glaucoma-risk gene (Nair et al. 2021).
The role of GLIS1 in reprogramming fibroblasts and other somatic cells to iPSCs have been established, where several methods can be developed using the potential of GLIS1 for producing clinically safe iPSCs for disease modeling and transplantation applications (Borgohain et al. 2019; Dey et al. 2021a, 2022; Haridhasapavalan et al. 2019; Saha et al. 2018). Cell-permeant version of GLIS1 (Dey et al. 2021b) along with OCT4 (Dey et al. 2021c), SOX2 (Thool et al. 2021), NANOG (Thool et al. 2022b), and other reprogramming factors (Raina et al. 2021; Thool et al. 2022a) can be used to derive clinical grade iPSCs for cell therapeutic applications. It is found to replace the proto oncogenes c-MYC and KLF4 in Yamanaka cocktail, thus making it an important factor in reprogramming. The ability of GLIS1 in iPSC production also sheds light about its endogenous role in multipotent stem cells other than pluripotent ESCs (Gérard et al. 2019). GLIS1 is a mesenchymal key transcription factor that is controlled by dynamic cell type–specific super-enhancers that become repressed in both lineages (Gérard et al. 2019). GLIS1 can control differentiation-induced genes; moreover, its overexpression can inhibit the lineage commitment of specific multipotent cells (Gérard et al. 2019). GLIS1 was identified as a central regulator of mesenchymal potency, and it was found to have an important role in adipogenesis (Gérard et al. 2019). Therefore, it is suggested that GLIS1 might contribute to the maintenance of the multipotent state in human development.
The exact mechanisms by which GLIS1 helps in increasing the reprogramming efficiency have not been reported. Online bioinformatics tools can be used for predicting the gene network and structure, which can help researchers identify interacting partners of GLIS1. Although GLIS1 is closely related to GLI-like protein subfamily, an insight into the role of its interacting proteins might give more information about the mechanisms and other roles of GLIS1. The identification of a single nucleotide polymorphism of GLIS1 gene is linked to Parkinson’s disease and that GLIS1 gene is located in PARK10 loci suggests the association of GLIS1 with Parkinson’s disease even though the gene involvement is unclear (Song et al. 2012). Also, studies can be conducted to find the association of GLIS1 gene in diseases other than cancer. Other members of the GLIS family are found to be associated with primary ciliogenesis, while the connection between GLIS1 and primary cilium has to be established. Targeting GLIS1 in tissues where it is overexpressed and lead to tumor formation can be a potential strategy to help in improving the efficacy of treating cancer. In this review, the multifaceted role of GLIS1 in embryonic development, cancer, and iPSCs is highlighted. The availability of secondary antibodies and unveiling the physiological mechanism would make GLIS1 to be utilized in the fields of stem cell biology, reprogramming, cancer, and other diseases and understanding the exact role in these areas of research.
Abbreviations
- ALL:
-
Acute lymphoblastic leukemia
- CAFs:
-
Cancer-associated fibroblasts
- CF:
-
Cystic fibrosis
- CFTR:
-
Cystic fibrosis transmembrane conductance regulator
- EMT:
-
Epithelial–mesenchymal transition
- ESCs :
-
Embryonic stem cells
- HTT :
-
Hyalinizing trabecular tumor
- iPSCs :
-
Induced pluripotent stem cells
- MET :
-
Mesenchymal–epithelial transition
- OSKMG :
-
OCT4, SOX2, KLF4, c-MYC, and GLIS1
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Ronima K R, Dey, C., Thummer, R.P. (2023). An Insight into the Role of GLIS1 in Embryonic Development, iPSC Generation, and Cancer. In: Advances in Experimental Medicine and Biology(). Springer, Cham. https://doi.org/10.1007/5584_2023_793
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