Interaction of the mTERT telomerase catalytic subunit with the c-Abl tyrosine kinase in mouse granulosa cells

References

• Chronowska E. Regulation of telomerase activity in ovarian granulosa cells. Indian J Exp Biol. 2012;50(9):595–601.
   PubMed Web of Science ®Google Scholar
• Cong YS, Wen J, Bacchetti S. The human telomerase catalytic subunit hTERT: organization of the gene and characterization of the promoter. Hum Mol Genet. 1999;8(1):137–142.
   PubMed Web of Science ®Google Scholar
• Misiti S, Nanni S, Fontemaggi G, et al. Induction of hTERT expression and telomerase activity by estrogens in human ovary epithelium cells. Mol Cell Biol. 2000;20(11):3764–3771.
   PubMed Web of Science ®Google Scholar
• Wang Z, Kyo S, Takakura M, et al. Progesterone regulates human telomerase reverse transcriptase gene expression via activation of mitogen-activated protein kinase signaling pathway. Cancer Res. 2000;60(19):5376–5381.
   PubMed Web of Science ®Google Scholar
• Brenner CA, Wolny YM, Adler RR, et al. Alternative splicing of the telomerase catalytic subunit in human oocytes and embryos. Mol Hum Reprod. 1999;5(9):845–850.
   PubMed Web of Science ®Google Scholar
• Wojtyla A, Gladych M, Rubis B. Human telomerase activity regulation. Mol Biol Rep. 2011;38(5):3339–3349.
   PubMed Web of Science ®Google Scholar
• Bakalova R, Ohba H, Zhelev Z, et al. Antisense inhibition of Bcr-Abl/c-Abl synthesis promotes telomerase activity and upregulates tankyrase in human leukemia cells. FEBS Lett. 2004;564(1–2):73–84.
   PubMed Web of Science ®Google Scholar
• Meltser V, Ben-Yehoyada M, Shaul Y. c-Abl tyrosine kinase in the DNA damage response: cell death and more. Cell Death Differ. 2011;18(1):2–4.
   PubMed Web of Science ®Google Scholar
• Bakalova R, Ohba H, Zhelev Z, et al. Cross-talk between Bcr-Abl tyrosine kinase, protein kinase C and telomerase-a potential reason for resistance to Glivec in chronic myelogenous leukaemia. Biochem Pharmacol. 2003;66(10):1879–1884.
   PubMed Web of Science ®Google Scholar
• Laneuville P. Abl tyrosine protein kinase. Semin Immunol. 1995;7(4):255–266.
   PubMedGoogle Scholar
• O’Neill AJ, Cotter TG, Russell JM, et al. Abl expression in human fetal and adult tissues, tumours, and tumour microvessels. J Pathol. 1997;183:325–329.
   PubMed Web of Science ®Google Scholar
• Shaul Y, Ben-Yehoyada M. Role of c-Abl in the DNA damage stress response. Cell Res . 2005;15(1):33–35.
   PubMed Web of Science ®Google Scholar
• Kharbanda S, Ren R, Pandey P, et al. Activation of the c-Abl tyrosine kinase in the stress response to DNA-damaging agents. Nature. 1995;376(6543):785–788.
   PubMed Web of Science ®Google Scholar
• Hantschel O, Superti-Furga G. Regulation of the c-Abl and Bcr-Abl tyrosine kinases. Nat Rev Mol Cell Biol. 2004;5(1):33–44.
   PubMed Web of Science ®Google Scholar
• Plattner R, Kadlec L, DeMali KA, et al. c-Abl is activated by growth factors and Src family kinases and has a role in the cellular response to PDGF. Genes Dev. 1999;13(18):2400–2411.
   PubMed Web of Science ®Google Scholar
• Ahmad K, Naz RK. Protein phosphorylation pattern and role of products of c-erbB-1 and c-abl proto-oncogenes in murine preimplantation embryonic development. Am J Reprod Immunol. 1994;32(3):226–237.
   PubMed Web of Science ®Google Scholar
• Yaba A, Kayisli UA, Johnson J, et al. The Abelson tyrosine kinase (c-Abl) expression on the mouse uterus and placenta during gestational period. J Mol Hist . 2011;42(2):91–96.
   PubMed Web of Science ®Google Scholar
• Li B, Boast S, de los Santos K, et al. Mice deficient in Abl are osteoporotic and have defects in osteoblast maturation. Nat Genet . 2000;24(3):304–308.
   PubMed Web of Science ®Google Scholar
• Hernandez SE, Krishnaswami M, Miller AL, et al. How do Abl family kinases regulate cell shape and movement? Trends Cell Biol. 2004;14:36–44.
   PubMed Web of Science ®Google Scholar
• Ucar AY, Kayisli UA, Demir N. The c-Abl expression in uterine epithelium during the mouse estrus cycle. J Mol Hist. 2012;43(1):107–113.
   PubMed Web of Science ®Google Scholar
• Russo V, Berardinelli P, Martelli A, et al. Expression of telomerase reverse transcriptase subunit (TERT) and telomere sizing in pig ovarian follicles. J Histochem Cytochem. 2006;54(4):443–455.
   PubMed Web of Science ®Google Scholar
• Lavranos TC, Mathis JM, Latham SE, et al. Evidence for ovarian granulosa stem cells: telomerase activity and localization of the telomerase ribonucleic acid component in bovine ovarian follicles. Biol Reprod. 1999;61(2):358–366.
   PubMed Web of Science ®Google Scholar
• Eppig JJ. Reproduction: oocytes Call, Granulosa Cells Connect. Curr Biol. 2018;28(8):R354–R356.
   PubMed Web of Science ®Google Scholar
• Nugent CI, Bosco G, Ross LO, et al. Telomere maintenance is dependent on activities required for end repair of double-strand breaks. Curr Biol. 1998;8(11):657–660.
   PubMed Web of Science ®Google Scholar
• Polotnianka RM, Li J, Lustig AJ. The yeast Ku heterodimer is essential for protection of the telomere against nucleolytic and recombinational activities. Curr Biol. 1998;8(14):831–834.
   PubMed Web of Science ®Google Scholar
• Laroche T, Martin SG, Gotta M, et al. Mutation of yeast Ku genes disrupts the subnuclear organization of telomeres. Curr Biol. 1998;8(11):653–656.
   PubMed Web of Science ®Google Scholar
• Taagepera S, McDonald D, Loeb JE, et al. Nuclear-cytoplasmic shuttling of C-ABL tyrosine kinase. Proc Natl Acad Sci USA. 1998;95(13):7457–7462.
   PubMed Web of Science ®Google Scholar
• Jones ASK, Shikanov A. Follicle development as an orchestrated signaling network in a 3D organoid. J Biol Eng. 2019;13(1):2.
   PubMedGoogle Scholar
• Liu YX, Zhang Y, Li YY, et al. Regulation of follicular development and differentiation by intra-ovarian factors and endocrine hormones. Front Biosci. 2019;24(5):983–993.
   Google Scholar
• Van Etten RA, Jackson P, Baltimore D. The mouse type IV c-abl gene product is a nuclear protein, and activation of transforming ability is associated with cytoplasmic localization. Cell. 1989;58(4):669–678.
   PubMed Web of Science ®Google Scholar
• Iannilli F, Zalfa F, Gartner A, et al. Cytoplasmic TERT associates to RNA granules in fully mature neurons: role in the translational control of the cell cycle inhibitor p15INK4B. PLoS One. 2013;8(6):e66602.
   PubMed Web of Science ®Google Scholar
• Chiodi I, Mondello C. Telomere-independent functions of telomerase in nuclei, cytoplasm, and mitochondria. Front Oncol. 2012;2:133.
   PubMedGoogle Scholar
• Stampfer MR, Garbe J, Levine G, et al. Expression of the telomerase catalytic subunit, hTERT, induces resistance to transforming growth factor beta growth inhibition in p16INK4A(-) human mammary epithelial cells. Proc Natl Acad Sci USA. 2001;98(8):4498–4503.
   PubMed Web of Science ®Google Scholar
• Lindvall C, Hou M, Komurasaki T, et al. Molecular characterization of human telomerase reverse transcriptase-immortalized human fibroblasts by gene expression profiling: activation of the epiregulin gene. Cancer Res. 2003;63(8):1743–1747.
   PubMed Web of Science ®Google Scholar
• Geserick C, Tejera A, Gonzalez-Suarez E, et al. Expression of mTert in primary murine cells links the growth-promoting effects of telomerase to transforming growth factor-beta signaling. Oncogene. 2006;25(31):4310–4319.
   PubMed Web of Science ®Google Scholar
• Kharbanda S, Kumar V, Dhar S, et al. Regulation of the hTERT telomerase catalytic subunit by the c-Abl tyrosine kinase. Curr Biol. 2000;10(10):568–575.
   PubMed Web of Science ®Google Scholar
• Tybulewicz VL, Crawford CE, Jackson PK, et al. Neonatal lethality and lymphopenia in mice with a homozygous disruption of the c-abl proto-oncogene. Cell. 1991;65(7):1153–1163.
   PubMed Web of Science ®Google Scholar
• Kharbanda S, Yuan ZM, Weichselbaum R, et al. Determination of cell fate by c-Abl activation in the response to DNA damage. Oncogene. 1998;17(25):3309–3318.
   PubMed Web of Science ®Google Scholar
• Kharbanda S, Pandey P, Morris PL, et al. Functional role for the c-Abl tyrosine kinase in meiosis I. Oncogene. 1998;16(14):1773–1777.
   PubMed Web of Science ®Google Scholar
• Yamagata Y, Nakamura Y, Umayahara K, et al. Changes in telomerase activity in experimentally induced atretic follicles of immature rats. Endocr J. 2002;49(6):589–595.
   PubMed Web of Science ®Google Scholar
• Chen H, Wang W, Mo Y, et al. Women with high telomerase activity in luteinised granulosa cells have a higher pregnancy rate during in vitro fertilisation treatment. J Assist Reprod Genet. 2011;28(9):797–807.
   PubMed Web of Science ®Google Scholar
• Tomanek M, Chronowska E, Kott T, et al. Telomerase activity in pig granulosa cells proliferating and differentiating in vitro. Anim Reprod Sci. 2008;104:284–298.
   PubMed Web of Science ®Google Scholar
• Bayne S, Li H, Jones ME, et al. Estrogen deficiency reversibly induces telomere shortening in mouse granulosa cells and ovarian aging in vivo. Protein Cell. 2011;2:333–346.
   PubMed Web of Science ®Google Scholar
• Liao XH, Lu DL, Wang N, et al. Estrogen receptor alpha mediates proliferation of breast cancer MCF-7 cells via a p21/PCNA/E2F1-dependent pathway. FEBS J. 2014;281(3):927–942.
   PubMed Web of Science ®Google Scholar
• Wang C, Yu J, Kallen CB. Two estrogen response element sequences near the PCNA gene are not responsible for its estrogen-enhanced expression in MCF7 cells. PLoS One. 2008;3(10):e3523.
   PubMed Web of Science ®Google Scholar
• Zhao H, Chen MS, Lo YH, et al. The Ron receptor tyrosine kinase activates c-Abl to promote cell proliferation through tyrosine phosphorylation of PCNA in breast cancer. Oncogene. 2014;33(11):1429–1437.
   PubMed Web of Science ®Google Scholar
• He X, Wei C, Song T, et al. Proliferating cell nuclear antigen destabilizes c-Abl tyrosine kinase and regulates cell apoptosis in response to DNA damage. Apoptosis. 2009;14(3):268–275.
   PubMed Web of Science ®Google Scholar
• Liu W, Zhu GJ. [Expression of telomerase in human ovarian luteinized granulosa cells and its relationship to ovarian function]. Zhonghua Fu Chan Ke Za Zhi. 2003;38(7):402–404.
   PubMedGoogle Scholar
• Xu X, Chen X, Zhang X, et al. Impaired telomere length and telomerase activity in peripheral blood leukocytes and granulosa cells in patients with biochemical primary ovarian insufficiency. Hum Reprod. 2017;32(1):201–207.
   PubMed Web of Science ®Google Scholar
• Butts S, Riethman H, Ratcliffe S, et al. Correlation of telomere length and telomerase activity with occult ovarian insufficiency. J Clin Endocrinol Metab. 2009;94(12):4835–4843.
   PubMed Web of Science ®Google Scholar
• Maser RS, DePinho RA. Keeping telomerase in its place. Nat Med . 2002;8(9):934–936.
   PubMed Web of Science ®Google Scholar
• Wong JM, Kusdra L, Collins K. Subnuclear shuttling of human telomerase induced by transformation and DNA damage. Nat Cell Biol . 2002;4(9):731–736.
   PubMed Web of Science ®Google Scholar
• Varela E, Sanchez-de-Puerta I, Garcia-Velasco JA. Fertility, IVF and reproductive genetics. Curr Opin Obstet Gynecol. 2018;30:203–208.
   PubMed Web of Science ®Google Scholar
• Rocca MS, Foresta C, Ferlin A. Telomere length: lights and shadows on their role in human reproduction. Biol Reprod. 2019;100(2):305–317.
   PubMed Web of Science ®Google Scholar
• Liu JP, Li H. Telomerase in the ovary. Reproduction. 2010;140(2):215–222.
   PubMed Web of Science ®Google Scholar
• Yaba A, Demir N. The mechanism of mTOR (mammalian target of rapamycin) in a mouse model of polycystic ovary syndrome (PCOS). J Ovarian Res. 2012;5(1):38.
   PubMedGoogle Scholar