Mingliang Yi1†
Hongguo Cao- 1Anhui Province Key Laboratory of Local Livestock and Poultry Genetic Resource Conservation and Bio-breeding, Anhui Agricultural University, Hefei, China
- 2College of Animal Science and Technology, Anhui Agricultural University, Hefei, China
Telomerase determines cell lifespan by controlling chromosome stability and cell viability, m6A epigenetic modification plays an important role in the regulation of telomerase activity. Using CRISPR epigenome editing to analyze specific m6A modification sites in telomerase will provide an important tool for analyzing the molecular mechanism of m6A modification regulating telomerase activity. In this review, we clarified the relevant applications of CRISPR system, paid special attention to the regulation of m6A modification in stem cells and cancer cells based on CRISPR system, emphasized the regulation of m6A modification on telomerase activity, pointed out that m6A modification sites regulate telomerase activity, and discussed strategies based on telomerase activity and disease treatment, which are helpful to promote the research of anti-aging and tumor related diseases.
1 Introduction
The research of telomere and telomerase is of great significance to the aging of organism. Telomerase is an eukaryotic ribonucleoprotein (RNP) composed of RNA-protein complex (Blackburn and Collins, 2011). It extends the 3‘end of linear chromosome by synthesizing the telomere repeat TTAGGG to maintain telomere length and chromosome stability (Liu et al., 2022). Telomerase activity is closely related to tumorigenesis (Shay, 2016; Trybek et al., 2020), cell proliferation and cell aging (Chakravarti et al., 2021). N6-methyladenosine (m6A) RNA modification is an important epigenetic modification mode in post-transcriptional regulation (Schmidt et al., 1975; Roundtree et al., 2017a; Tang et al., 2020), which involves almost all aspects of RNA metabolism and affects various physiological and pathological processes by regulating mRNA cytoplasmic transport, splicing, stability, structure and translation (Dominissini et al., 2012). The composition of telomerase fully shows that it has a close relationship with m6A modification. The study of the mechanism of m6A modification regulating telomerase activity and maintaining telomere length will promote human anti-aging to provide new ideas.
With the application and improvement of CRISPR (clustered regularly interspaced short palindromic repeats)/Cas system (Jinek et al., 2012; Cong et al., 2013), the modified fusion protein dm6ACRISPR system can achieve precise and efficient m6A site-specific modification in RNA transcripts (Liu et al., 2019; Wilson et al., 2020), this will help to further explore the mechanism of m6A modification. In clinical cancer research, it was found that there was a site mutation in the promoter region of telomerase reverse transcriptase (TERT) gene. Use the base editing function of CRISPR system to reduce the transcription and protein expression of TERT, and induce the aging and proliferation stagnation of cancer cells, which verifies the feasibility of activated TERT promoter mutation as a cancer-specific therapeutic target (Killela et al., 2013; Li et al., 2020). Therefore, the CRISPR system technology, combined with the m6A modification of RNA and the regulation of telomerase activity, is used to regulate the aging and proliferation of cells in the body and achieve the treatment of various diseases.
In this review, we reviewed and discussed the latest research progress, and found that the CRISPR system was used to carry out m6A site-specific modification of RNA, regulate telomerase activity and affect telomere length by regulating telomerase assembly and other processes, which provided a direction for the study of epigenetic modification to regulate cell aging mechanism, and provided a prospect for the future research on cell proliferation and aging.
2 CRISPR system introduction
CRISPR/Cas9 system widely exists in prokaryotes and provides acquired immunity against the invasion of foreign viruses and plasmids (Ghaemi et al., 2021). The developed CRISPR/Cas system can accurately edit DNA or RNA targets at specific sites and has been widely used in gene editing (Hsu et al., 2014; Manghwar et al., 2019; Zhang et al., 2021). According to the composition of Cas effector proteins, CRISPR system is divided into Class I and Class II (Figure 1). These systems use site-specific guide RNA to guide Cas protein and accurately edit site-specific sequences (Wang et al., 2022; Yu et al., 2022). At present, the most widely used CRISPR systems are Class II Type II Cas9, Type V Cas12 and Type VI Cas13 (Figure 1).
FIGURE 1. CRISPR/Cas system classification, typical structure, important members of Class II CRISPR/Cas system and principle of CRISPR/Cas system. (A) The structure of class I and class II CRISPR/Cas system loci. The class I of CRISPR/Cas system is composed of multiple Cas proteins to form a crRNA complex, which plays a role in the binding and processing of targets; The class II of CRISPR/Cas system is composed of a single multi-domain crRNA-binding protein, and its function is similar to the effect complex in the class I of CRISPR system. (B) CRISPR/Cas9 system is mainly composed of Cas9 protein and single-stranded guide RNA (sgRNA). Cas9 protein has the function of cutting DNA double-stranded, and sgRNA plays a guiding role. In the presence of the adjacent motif (PAM) of the prototype spacer, Cas9 protein can reach different target sites through base complementary pairing under the guidance of sgRNA, and achieve DNA double strand break (DSB) by cutting the target gene through the two nuclease domains of RuvC and HNH. (C) CRISPR/Cas12 system is mainly composed of Cas12 protein and single-stranded guide RNA (sgRNA). Cas12 protein has side-cutting activity and can cut double and single strands of DNA. It mainly plays the role of inducing DSBs through a single RuvC-like nuclease domain. (D) CRISPR/Cas13 system is mainly composed of Cas13 protein and single-stranded guide RNA (sgRNA). Cas13 protein is a single protein composed of multiple domains. It has the function of recognizing crRNA, cutting RNA, and even cutting pre-crRNA. It has the phenomenon of side-cutting activity similar to CRISPR/Cas12 system. It cuts RNA through two HEPN domains. (E) CRISPR/Cas system is an acquired immune system from bacteria and archaea. Taking the principle of CRISPR/Cas9 system as an example: the acquisition of highly variable spacer of CRISPR - the expression of CRISPR loci (transcription and post-transcriptional maturation) - the development of CRISPR/Cas9 system activity.
The CRISPR system is mainly used to modify specific target genes in the genome of organisms. The main editors include DNA cytosine base editor (CBE), adenine base editor (ABE) and primer editor (PE) (Kantor et al., 2020). PE is a multi-functional and high-precision genome editor (Anzalone et al., 2019), which is composed of two parts: the leader editor protein and primer editing guided RNA (pegRNA). Using the CRISPR Cas protein targeted DNA to make nicks and the DNA synthesis ability of reverse transcriptase, the sequence encoded by pegRNA can be accurately and efficiently copied into the targeted DNA sequence to achieve accurate editing, including replacement, insertion and deletion (Anzalone et al., 2019; Kantor et al., 2020; Kim et al., 2020). The advantage of PE is that it does not cause DNA double strand breakage, only cutting one strand of DNA, thereby avoiding potential risks such as chromosome loss and rearrangement caused by double strand DNA breakage. Researchers can further improve the accuracy and specificity of PE by optimizing lead editing proteins, pegRNA, and AAV genomic elements, such as introducing engineered Cas9 mutants, especially eSpCas9 and Sniper Cas9 mutants, into PE (Kim et al., 2020). The PE editing efficiency prediction models DeepPrime, DeepPrime FT, and the off target prediction model DeepPrime Off make the design and screening of pegRNAs more convenient and efficient, providing strong guarantees for the future widespread application of PE systems (Yu et al., 2023). Using PE to repair sickle cell anemia (SCD) mutations in hematopoietic stem cells or progenitor cells of patients, the repaired cells are treated for hereditary blood diseases through transplantation (Everette et al., 2023). The gene editing system developed based on CRISPR technology has brought prospects for the research and treatment of genetic diseases.
3 CRISPR system and RNA editing
At present, CRISPR/Cas9 and CRISPR/Cas13 systems have become tools for the research and application of DNA and RNA epigenetic modification (Figure 2; Figure 3) (Zhan et al., 2019; Kordyś et al., 2022). Nucleic acid endonuclease deficient Cas9 (dCas9)/Cas13 (dCas13) still has the activity of binding enzyme, which can combine with effector protein to regulate the expression of DNA or RNA, becoming an effective method to study gene function and regulation mechanism (Yang et al., 2019; Liu et al., 2020).
FIGURE 2. DNA editing tools-CRISPR/dCas9.
FIGURE 3. CRISPR system in RNA editing applications.
Working principle of CRISPR/dCas9 system and related tools based on CRISPR/dCas9 system development (gene editing, live cell imaging, base editing, methylation modification, histone modification and transcription regulation). Ac, acetylation; Me, Methylation; Dme, Demethylation.
3.1 RNA editing tools: based on CRISPR/dCas13 system
The modification of CRISPR system for gene editing at the DNA level is irreversible, especially the ethical issues involved in the safety of human germ cell and embryonic cell editing cannot be ignored (Leibowitz et al., 2021; Höijer et al., 2022). p53 gene is a tumor suppressor gene that participates in the regulation of cell growth, differentiation, apoptosis and other processes (Fischer et al., 2016). After Cas9 protein was introduced into cells to realize CRISPR/Cas9 mediated genome editing, p53 pathway was upregulated and DNA repair level was increased. Cas9 protein induces p53 pathway activation and p53 mediated DNA damage response (Enache et al., 2020). These findings are of great significance for the correct application of CRISPR/Cas9 mediated genome editing (Enache et al., 2020; Sinha et al., 2021). Therefore, the use of CRISPR/Cas9 technology in human pluripotent stem cells (hPSCs) cell replacement therapy should be carefully carried out and the p53 function of hPSCs cells should be monitored (Ihry et al., 2018). The modification of Cas13 protein at the RNA level successfully avoids irreversible permanent changes to the genome, and is an important tool for studying the most abundant m6A modification on RNA. At the same time, it plays an important role in studying the structure and function of telomerase composed of RNA and protein.
In terms of RNA editing, the CRISPR system has been deeply modified and applied to mRNA epigenetic modification research. The m1A modification detection method based on the CRISPR/Cas13a system has been successfully used to identify m1A in 28S rRNA (Chen et al., 2019). The catalytic inactivation of RfxCas13d (dCasRx) is fused with the m1A demethylase ALKBH3, and the dCasRx ALKBH3 fusion protein can mediate effective demethylation of m1A modified RNA, known as Reengined m1A modification valid eraser (“REVER”), providing a tool for further elucidating the relationship between m1A modification of specific transcripts and their phenotypic results (Xie et al., 2021). m1A regulates the level of glycolysis in tumor cells by regulating the expression of ATP5D in the mitochondrial ATP synthase F1 domain. The dm1ACRISPR system can upregulate the expression of ATP5D through targeted removal of ATP5D m1A modification, resulting in an increase in the level of glycolysis of tumor cells (Wu et al., 2022). This is similar to using the CRISPR system to study m6A modification, where endogenous editing studies can be conducted by identifying the targets of epigenetic modifications on mRNA such as m1A and m5C. Because the CRISPR/RfxCas13d (CasRx) related transcriptome epigenetic modification editor has the characteristics of small size and high editing efficiency (Konermann et al., 2018; Zhang et al., 2018), which is suitable for packaging into lentivirus vector for gene function research. At present, CasRx has been successfully used to knock down specific mRNA transcripts in zebrafish embryos (Kushawah et al., 2020), and to mediate RNA targeted treatment of age-related macular degeneration in model mice (Zhou et al., 2020).
4 CRISPR system and m6A modification
As an important biological function of RNA modification, m6A modification widely exists in almost all types of RNA molecules in cells (Yang et al., 2018; Hu et al., 2022). In the regulation of m6A modification, combining the modified protein specific domain with the inactivated CRISPR protein can produce a new precise editing tool for RNA methylation modification (Figure 4) (Li et al., 2020; Wilson et al., 2020; Kordyś et al., 2022). Liu et al. designed m6A modified eraser by combining CRISPR/Cas9 with demethylase ALKBH5 or FTO to realize RNA site-specific demethylation (Liu et al., 2019). Considering the important regulatory role of m6A modification on RNA in the nucleus, based on the RNA-targeted endonuclease system CRISPR/Cas13, an editor for targeted RNA methylation (TRM) was constructed, which became a new accurate editing tool for m6A modification. The editor can achieve efficient and accurate editing of m6A modification of RNA in nucleus and cytoplasm through nuclear export-signal (NES) and nuclear localization signal (NLS) (Wilson et al., 2020). The dm6ACRISPR editing tool can realize m6A modification of RNA sites, providing a more powerful weapon for in-depth research on the function of m6A modification (Table 1).
FIGURE 4. CRISPR system and m6A modification (A) N6-methyladenosine (m6A) regulation mechanism. Writers and erasers strictly regulate the presence of m6A on transcripts by targeting the m6A motif (DRACH). m6A is recognized by readers and starts the steps of regulating mRNA stability and translation. The modification system can be extended to include Cas9 (base editor, writer/eraser fusion) and Cas13 (methylation system). (B) Application of CRISPR/dCas9-ALKBH5/FTO tool in m6A modification. (C) Application of CRISPR/dCas13-Writer Complex tool in m6A modification; Application of CRISPR/dCas13-ALKBH5/FTO tool in m6A modification.
TABLE 1. Application of CRISPR system associated key regulatory factors in m6A modification.
5 CRISPR system and telomerase
Telomerase, as an enzymatic RNP complex, plays a role of reverse transcriptase in the process of telomere elongation, and is significantly associated with cell aging and tumorigenesis (Sun et al., 2019). In cancer cells (Bajaj et al., 2020; Negrini et al., 2020; Wu et al., 2020), hematopoietic stem cells (Celtikci et al., 2021) and germ cells (Dogan and Forsyth, 2021; Lupatov and Yarygin, 2022), telomerase showed high activity (Demanelis et al., 2020). Cancer is closely related to a series of changes in intracellular genome and epigenome (Ushijima et al., 2021). Telomerase is silent in most normal somatic cells, but activated in 90% of cancer cells, making it an excellent target for cancer treatment. In the treatment of cancer, all kinds of telomerase activity inhibitors have failed due to their side effects. Coats plus (CP) is a rare autosomal recessive disease caused by CTC1 mutation, which is important for maintaining telomere length. CTC1L1142H mutation caused telomere damage. The point mutation of CTC1 using CRISPR/Cas9 technology confirmed that the interaction between CTC1 and STN1 is necessary to inhibit telomerase activity (Gu et al., 2018). Combining the biological functions of CRISPR/Cas9 and telomerase, the development of telomerase activating gene expression (Tage) has gradually become a new cancer gene therapy method. The Tage system consists of three components: the effector gene expression vector carrying 3‘telomerase recognition rod end, the dCas9-VP64 expression vector and the sgRNA artificial transcription factor expression vector targeting the telomere repeat sequence. Using AAV as a gene vector, the Tage system can effectively kill cancer cells and safely realize its application in the body (Dai et al., 2019). In cancer research using CRISPR system, CRISPR activation screening of targeted gRNA was carried out, gRNA libraries targeting different genes were established, targeted genes in cancer cells were systematically and accurately knocked out, and cancer gene therapy was achieved (Joung et al., 2022; Katti et al., 2022; Ye et al., 2022).
Telomerase activity usually depends on the expression level of TERT, which is the catalytic subunit of RNP complex (Barthel et al., 2017; Wu et al., 2021). The recruitment of telomerase to telomere occurs in the S phase of the cell cycle. By using CRISPR genome editing system and CRISPR-aided nano microscope technology to track telomerase in the nucleus, it is proved that telomerase uses three-dimensional diffusion to search for telomeres, and the recruitment of telomerase to telomere is driven by the dynamic interaction between the rapidly diffusing telomerase protein TERT and telomere protein TPP1 (Schmidt et al., 2016). In the study of human telomerase RNA (hTR) biogenic post-transcriptional modification, the use of CRISPR system consumes trimethyl guanosine synthetase 1 (TGS1). The reduction of trimethylation will increase the coupling of hTR with cap-binding complex (CBC) and Sec1/Munc-18 (Sm) chaperone protein, The accumulation of mature hTR in the nucleus and cytoplasm increases, and the increased hTR is assembled with TERT protein to produce increased active telomerase complex and increased telomerase activity, thus realizing the telomere elongation of cultured human cells. This study provides a new treatment scheme for telomerase dysfunction in telomeric syndrome (Figure 5) (Chen et al., 2020).
FIGURE 5. Application of CRISPR/Cas9 system in regulating telomerase and telomere (A) Use CRISPR/Cas9 and CRISPR/dCas9 systems to cut telomeres through telomerase to produce DNA damage and induce cancer cell death. (B) Use CRISPR/Cas9 system to introduce TGS1 gene frameshift mutation to realize the deletion of TGS1 hypermethylation enzyme and promote the increase of telomerase RNA and telomere elongation.
In order to further study the activation of telomerase and its activity regulation mechanism, in view of the low editing efficiency of CRISPR/Cas9 at the TERT gene locus, the genome editing method of “pop in/pop out” is used to realize precise modification of endogenous TERT gene sites in cells. This method provides a powerful tool for studying the biological function of telomerase using CRISPR/Cas9 (Kühn and Chu, 2015; Xi et al., 2015). Thus, the emergence of CRISPR system will provide an important tool for human research on telomerase and the regulation mechanism of cell aging.
6 dm6ACRISPR system and telomerase
As a repeat DNA sequence at the end of chromosome, telomere shortening is considered as a biological marker of cell aging (Al-Turki and Griffith, 2023). At each cell division, 50–100 pairs of base pairs will be lost in the chromosome end sequence, resulting in cell aging and even death (Blasco, 2005; Rossiello et al., 2022). Telomerase contains specialized TERT and telomerase RNA (TER), and has its own template and catalytic core required by TERT (Cash and Feigon, 2017; Jiang et al., 2018; Wang et al., 2019). In most human cancers, the increase of telomerase level makes cancer cells have the ability to proliferate indefinitely (Roake and Artandi, 2020). According to the characteristics of telomerase structure, composition and epigenetic modification (Figure 6; Figure 7), the telomere repeat sequence at the end of chromosome is extended to maintain the stability of genome, and the gradual loss of telomere caused by genome replication is offset. These are important for studying cell proliferation and delaying cell aging (He et al., 2021; Liu et al., 2022; Sekne et al., 2022).
FIGURE 6. Telomerase.
FIGURE 7. Relationship between telomeres and telomerase (A) Cell proliferation and telomere length reduction. Telomere is a repetitive DNA structure at the top of the chromosome. When the cell division DNA replicates, the telomere will protect the integrity of the chromosome. The activity of telomerase in normal cells was inhibited, and the telomere gradually shortened and disappeared with the continuous cell division. Chromosomes are finally completely exposed, cells cannot proliferate, DNA molecules degrade, and life ends. (B) The life cycle of telomerase and its regulation mechanism. Telomerase-protein RNA complex uses the non-coding RNA subunit hTR as a template, and the reverse transcriptase TERT catalyzes the telomere elongation. The life cycle of telomerase includes post-transcriptional modification (PTM) and maturation of hTR, intracellular localization, and effective assembly with TERT until the formation of a whole enzyme that can prolong telomeres.
The abnormal modification of RNA methylation is closely related to a series of cancer occurrence, and studying the relationship between m6A modification and tumor occurrence is of great significance for the treatment of cancer. In liver cancer research, it was found that methyltransferase METTL14 has a dual effect of promoting cancer cell proliferation and differentiation and inhibiting cancer cell metastasis (Ma et al., 2017; Chen et al., 2018); Overexpression of METTL5 promotes the growth, proliferation, migration, and invasion of liver cancer, knockdown of METTL5 promotes cell apoptosis, and inhibits the growth, proliferation, migration, and invasion of liver cancer (Peng et al., 2022). METTL3 has carcinogenic function in human liver cancer, and downregulation of METTL3 can weaken the tumorigenicity and lung metastasis of liver cancer (Chen and Wong, 2020). In glioblastoma, METTL3 can promote the maintenance and radiation resistance of glioblastoma stem cells and inhibit their self-renewal and proliferation (Cui et al., 2017; Visvanathan et al., 2018). Inhibition of FTO expression can hinder the growth, differentiation and self-renewal of glioblastoma stem cells (Cui et al., 2017). ALKBH5 can promote stem cell self-renewal and proliferation (Zhang et al., 2017). Overexpression of ALKBH5 was found in breast cancer research to enhance the enrichment of breast cancer stem cells (BCSC) (Zhang et al., 2016). In lung cancer and bladder cancer, METTL3 knockout can reduce the growth, survival and invasiveness of lung cancer cells, as well as the proliferation, invasion, in vitro survival and in vivo tumorigenicity of bladder cancer cells (Lin et al., 2016; Han et al., 2019). The m6A modification is closely related to the occurrence of cancer, and the m6A editing tool based on the CRISPR system will help to analyze the correlation mechanism between m6A modification and cancer occurrence.
At present, the dm6ACRISPR editing tool is constructed by combining the catalytically inactivated Cas protein with the m6A modification related protein (Li et al., 2020). This laid a foundation for studying the relationship between epigenetic modification and telomerase function and exploring the mechanism of m6A modification on telomerase activity regulation.
Telomerase structure. Telomerase is a ribonucleoprotein complex, which is composed of scaffold non-coding human telomerase RNA (hTR), telomerase reverse transcriptase (TERT) and related cofactors. Telomerase is composed of two RNA-linked structures. One is the H/ACA domain of hTR, which is composed of two groups of dyskerin complex (dyskerin, NHP2, NOP10 and GAR1) and TCAB1. The other contains the catalytic core, where hTR and TERT surround the telomere substrate. The two are connected through the CR4/5 domain of hTR.
6.1 Regulation of telomerase activity by m6A modification
RNA epigenetic modifications commonly include 5-methylcytidine (m5C) (Bohnsack et al., 2019), N6-methyladenosine (m6A) (Oerum et al., 2021), N7-methylguanosine (m7G) (Malbec et al., 2019), N1-methyladenosine (m1A) (Zhou et al., 2019), inosine (I) (Srinivasan et al., 2021), and pseudo uracil (Ψ) And dihydrouracil (D) (Haruehanroengra et al., 2020). m6A modification is closely related to many kinds of carcinogenesis, and altered m6A modification is widely involved in the progression of various tumorigenesis (Gu et al., 2020; Li et al., 2022). Deeply study m6A modification by regulating telomerase activity to maintain telomere homeostasis and genome stability is of great significance to clarify the role of m6A modification in cell aging and carcinogenesis (Table 2). Through Pan-Cancer Analysis of Whole Genomes (PCAWG) analysis of m6A modification of telomerase components, it was found that in most cancers, the expression level of telomerase components was positively correlated with methylase METTL3, negatively correlated with methylase METTL14, negatively correlated with demethylase FTO, negatively correlated with reading proteins YTHDC1, YTHDC2, YTHDF3 and FMR1, and positively correlated with reading proteins HNRNPC, HNRNP2B1, YTHDF1 and RBMX (Wang et al., 2023). These showed that there was a close relationship between telomerase component activity and m6A regulatory factors. With the help of the established CRISPR/dCas13 system to accurately edit the m6A modification platform, it is proved that the METTL3-HMBOX1 axis regulates telomere recruitment and telomere length related to telomerase in cancer cells, and leads to DNA damage reaction (Figure 8) (Lee et al., 2021). METTL3 promotes the stabilization of p53 protein and the expression of target genes in response to DNA damage and carcinogenic signals through catalytic activity dependent and independent mechanisms (Zhao et al., 2020; Raj et al., 2022). In addition, METTL3-m6A-p53 axis may be a potential target for the treatment of hepatocellular carcinoma (HCC) (Ke et al., 2022). Therefore, we can use CRISPR system to modify specific target genes with m6A, and regulate telomerase activity by regulating p53 signal pathway to maintain telomere homeostasis (Figure 9).
TABLE 2. Function of m6A regulator in telomerase activity.
FIGURE 8. Application of m6A editing tool of dCas13b-METTL3 in telomerase activity regulation.
FIGURE 9. The mechanism of the m6A editing tool of CRISPR system to regulate telomerase activity and maintain telomere length in the p53 signal pathway.
dCas13b-METTL3, a m6A editing tool based on CRISPR system, proves that METTL3-catalyzed HMBOX1 methylation is involved in regulating telomerase recruitment, resulting in telomere loss in cancer cells, and m6A is involved in carcinogenesis.
The m6A editing tool of CRISPR system modifies mRNA with m6A, affects telomerase activity through p53 signal pathway, participates in phosphorylation of PKC and AKT or dephosphorylation of PP2A, telomere shortening leads to DNA damage, and activates p53 signal pathway.
Through its reading protein, m6A modification is widely involved in biological processes such as pre-mRNA splicing, RNA output, mRNA translation and RNA degradation, and regulates the stability of targeted mRNA (He and He, 2021). In the study of m6A reading protein, it was found that proteins containing YTH domain (YTHDF1 and YTHDC1) used YTH domain to recognize m6A modification, YTHDF1 and YTHDF3 worked together to affect the translation of m6A containing mRNA, YTHDF2 accelerated the decay of mRNA, and YTHDC1 affected the nuclear processing of its target, further regulating the function and fate of m6A labeled mRNA (Roundtree et al., 2017b; Hsu et al., 2017; Shi et al., 2017).
Knockout of YTHDF1 by CRISPR/Cas9 system will destroy the interaction between YT521-B homologous domain of YTHDF1 and AGO2 (argonaute 2), leading to the transformation of AGO2 droplets into gel/solids deposited in the cytoplasm (Li et al., 2022). In the nucleus, AGO2 interacts with 23 nt sRNA produced by TTS of telomerase RNA component telomerase RNA component (TERC) (position 425–447), which is called terc-sRNA. TERT and TERC constitute the core telomerase that maintains telomere length. As an RNA-binding protein, AGO2 has been found to promote telomerase activity and stimulate the association between TERT and TERC (Figure 10). AGO2 depletion leads to shorter telomeres and lower cell proliferation rate in vitro and in vivo (Laudadio et al., 2019). By regulating the recognition protein YTHDF1, it can regulate the consumption of AGO2 in the cytoplasm, affect the content of AGO2 in the nucleus, and lead to the change of telomerase activity in cells, which may lay the foundation for new therapeutic targets of tumor and telomeric diseases.
FIGURE 10. m6A reading protein and telomerase (A) The interaction between AGO2 and 23 nt sRNA produced by TTS of telomerase RNA component TERC (position 425–447) - terc-sRNA. (B) YTHDF1 interacts with AGO2 through YTH domain. YTHDF1 downregulates and destroys the interaction between YTHDF1 and AGO2. AGO2 deposits abnormally in the cytoplasm. AGO2 depletion destroys the association between TERT and TERC RNA, reduces telomerase activity, and leads to telomere shortening.
6.2 Site-directed modification of telomerase by dm6ACRISPR system
After CRISPR/Cas9 system, CRISPR/Cas13 system of type VI belongs to a known type that specifically binds and cleaves exogenous RNA (Abudayyeh et al., 2016; Shmakov et al., 2017; Smargon et al., 2017). CRISPR/Cas13 system can resist pathogenic RNA virus or regulate gene expression, and promote the knockout of mRNA, circular RNA and non-coding RNA (Wessels et al., 2020; Li et al., 2021). In addition, CRISPR/Cas13 system has been used for RNA modification in vivo, including editable regulation of selective splicing, A-to-I and C-to-U editing and m6A modification (O'Connell, 2019; Kordyś et al., 2022). Using CRISPR/Cas13 system, m6A can be added to specific RNA sites in a targeted way to achieve precise m6A modification at specific RNA sites. Since the methylation and demethylation process of m6A mainly occurs in the nucleus, two nuclear localization signal (NLS) peptides are added to dCasRx-METTL3 and dCasRx-ALKBH5 editors to realize the nuclear localization of the editing complex, which are called NLS-dCasRx-NLS-METTL3 and NLS-dCasRx-NLS-ALKBH5 (Xia et al., 2021). m6A methyltransferase METTL3 can increase the methylation modification level of telomerase related gene Cbf5 mRNA, promote its transcription and translation, and enhance telomerase activity (Jiang et al., 2021). As a nuclear protein reverse transcriptase, telomerase is composed of RNA template and catalytic protein (Wang et al., 2019). There is a 5-nt GGACU sequence with m6A common motif matching in the H/ACA scaRNA structure of hTR (Han et al., 2020), adenosine in the motif (A435) is located in the double stranded region of the RNA, suggesting that its secondary structure may be affected by m6A modification (Liu et al., 2015). The double stranded structure of the H/ACA scaRNA domain of hTR has been shown to be important for the assembly of telomerase complexes (Zhang et al., 2011). Overexpression of demethylase ALKBH5 leads to a decrease in the assembly efficiency of TCAB1 and DKC1 on telomerase, resulting in a decrease in telomerase activity. This may be mediated by modifying hTR to regulate telomerase assembly and function (Han et al., 2020).
If telomerase activity is regulated by m6A modification, we consider attempting to achieve precise regulation using the nuclear localization CRISPR system combined with dCasRx and NLS. Assuming that the NLS-dCasRx-NLS-METTL3 system overexpressing METTL3 promotes Cbf5 transcription and translation (Figure 11), enhancing telomerase activity, and using NLS-dCasRx-NLS-ALKBH5 overexpressing ALKBH5 to remove m6A modification on hTR, Studying the regulation of TCAB1 and DKC1 assembly on telomerase by m6A modification (Figure 12) provides new insights into the potential application of CRISPR based m6A modification in telomerase regulation.
FIGURE 11. Regulation of telomere by m6A modification of NLS-dCasRx-NLS-METTL3 system.
FIGURE 12. Regulation of telomerase assembly by m6A modification of NLS-dCasRx-NLS- ALKBH5 system m6A gene editing tool NLS-dCasRx-NLS-ALKBH5 locates dCasRx-ALKBH5 in the nucleus to achieve specific demethylation. Use the gene editing tool dCasRX-ALKBH5 to modify the m6A demethylation of telomerase hTR, regulate the assembly of telomerase components TCAB1 and DKC1, and reduce cell telomerase activity.
m6A gene editing tool NLS-dCasRx-NLS-METTL3 locates dCasRx-METTL3 in the nucleus to achieve specific methylation. Using the gene editing tool dCasRX-METTL3, the methylation modification level of Cbf5 mRNA was increased, the transcription and translation level of Cbf5 was enhanced, and Cbf5, as a component of telomere synthetase, increased telomere synthetase activity and regulated telomerase activity.
7 Conclusions and future prospects
CRISPR gene editing system, as the most revolutionary breakthrough in the field of biotechnology, is an unprecedented tool to cure human genetic diseases (Gillmore et al., 2021; Fox et al., 2022). m6A modification plays an important role in almost all-important biological processes (Liu et al., 2022; Boulias and Greer, 2022). Telomerase is highly active in stem cells, immune cells and germ cells to maintain telomere length (Jiang et al., 2018; Wan et al., 2021). Using CRISPR system to study the regulation mechanism of m6A modification on telomerase activity is of great significance for exploring the mechanism of cell proliferation and aging.
In this review, we systematically describe the latest application of CRISPR system in m6A modification and the regulation of telomerase activity, providing ideas for understanding the basic mechanism of regulating cell aging. When considering that m6A is the most common, frequent and conservative internal modification, and that telomerase activity is inhibited in normal cells, but remains high in most cancer cells, it is reasonable to propose that further exploring the mechanism of m6A modification on telomerase activity regulation will help to identify and develop gene therapy that can fight aging and treat cancer. It is now clear that the expression and activity of these proteins are essential for the correct regulation of the cell’s non-stop replication process. Strong evidence has emerged about the various functions of these proteins and the corresponding functions of targeted RNA in stem cells, immune cells, germ cells and sperm. So as we continue to decipher the epigenetic modification of m6A and the biology of cell proliferation and aging, we will have an important and in-depth understanding of the molecular mechanism of physiological and pathological cell aging.
Author contributions
MY, MW, YX, and ZC drafted the manuscript. YL, ZZ, and HG designed and revised the manuscript. All authors contributed to the article and approved the submitted version.
Funding
This research was partially supported by National Natural Science Foundation of China (project code: 32272875), Anhui Natural Science Foundation (project code: 2208085MC75) and Anhui Meat Sheep Joint Breeding Project (project code: 340000211260001000431).
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
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Keywords: CRISPR system, m6A modification, epigenetic regulation, telomere, telomerase
Citation: Yi M, Wang M, Xu Y, Cao Z, Ling Y, Zhang Z and Cao H (2023) CRISPR-based m6A modification and its potential applications in telomerase regulation. Front. Cell Dev. Biol. 11:1200734. doi: 10.3389/fcell.2023.1200734
Received: 05 April 2023; Accepted: 27 June 2023;
Published: 14 July 2023.
Edited by:
Guang Ji, Shanghai University of Traditional Chinese Medicine, ChinaReviewed by:
Haiwei Mou, Wistar Institute, United StatesXiao-Min Liu, China Pharmaceutical University, China
Copyright © 2023 Yi, Wang, Xu, Cao, Ling, Zhang and Cao. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Yinghui Ling, bGluZ3lpbmdodWlAYWhhdS5lZHUuY24=; Zijun Zhang, emhhbmd6aWp1bkBhaGF1LmVkdS5jbg==; Hongguo Cao, Y2FvaG9uZ2d1bzFAYWhhdS5lZHUuY24=
†These authors have contributed equally to this work