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GLIS1-3 转录因子:在调节多种生理过程和疾病中的关键作用。

GLIS1-3 transcription factors: critical roles in the regulation of multiple physiological processes and diseases.

机构信息

Cell Biology Group, Immunity, Inflammation and Disease Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, NC, 27709, USA.

出版信息

Cell Mol Life Sci. 2018 Oct;75(19):3473-3494. doi: 10.1007/s00018-018-2841-9. Epub 2018 May 19.

Abstract

Krüppel-like zinc finger proteins form one of the largest families of transcription factors. They function as key regulators of embryonic development and a wide range of other physiological processes, and are implicated in a variety of pathologies. GLI-similar 1-3 (GLIS1-3) constitute a subfamily of Krüppel-like zinc finger proteins that act either as activators or repressors of gene transcription. GLIS3 plays a critical role in the regulation of multiple biological processes and is a key regulator of pancreatic β cell generation and maturation, insulin gene expression, thyroid hormone biosynthesis, spermatogenesis, and the maintenance of normal kidney functions. Loss of GLIS3 function in humans and mice leads to the development of several pathologies, including neonatal diabetes and congenital hypothyroidism, polycystic kidney disease, and infertility. Single nucleotide polymorphisms in GLIS3 genes have been associated with increased risk of several diseases, including type 1 and type 2 diabetes, glaucoma, and neurological disorders. GLIS2 plays a critical role in the kidney and GLIS2 dysfunction leads to nephronophthisis, an end-stage, cystic renal disease. In addition, GLIS1-3 have regulatory functions in several stem/progenitor cell populations. GLIS1 and GLIS3 greatly enhance reprogramming efficiency of somatic cells into induced embryonic stem cells, while GLIS2 inhibits reprogramming. Recent studies have obtained substantial mechanistic insights into several physiological processes regulated by GLIS2 and GLIS3, while a little is still known about the physiological functions of GLIS1. The localization of some GLIS proteins to the primary cilium suggests that their activity may be regulated by a downstream primary cilium-associated signaling pathway. Insights into the upstream GLIS signaling pathway may provide opportunities for the development of new therapeutic strategies for diabetes, hypothyroidism, and other diseases.

摘要

Krüppel 样锌指蛋白构成了最大的转录因子家族之一。它们作为胚胎发育和广泛的其他生理过程的关键调节剂发挥作用,并与多种病理有关。GLI 样 1-3(GLIS1-3)构成了 Krüppel 样锌指蛋白家族的一个亚家族,它们可以作为基因转录的激活剂或抑制剂。GLIS3 在调节多种生物过程中起着关键作用,是胰腺β细胞生成和成熟、胰岛素基因表达、甲状腺激素生物合成、精子发生以及维持正常肾脏功能的关键调节剂。人类和小鼠中 GLIS3 功能的丧失会导致多种病理的发生,包括新生儿糖尿病和先天性甲状腺功能减退、多囊肾病和不育。GLIS3 基因中的单核苷酸多态性与多种疾病的风险增加有关,包括 1 型和 2 型糖尿病、青光眼和神经紊乱。GLIS2 在肾脏中起着关键作用,GLIS2 功能障碍导致肾单位肾病变,这是一种终末期、囊性肾病。此外,GLIS1-3 在几种干细胞/祖细胞群体中具有调节功能。GLIS1 和 GLIS3 极大地提高了体细胞重编程为诱导性胚胎干细胞的效率,而 GLIS2 则抑制了重编程。最近的研究获得了关于 GLIS2 和 GLIS3 调节的几个生理过程的大量机制见解,而对 GLIS1 的生理功能知之甚少。一些 GLIS 蛋白定位于初级纤毛,这表明它们的活性可能受到下游初级纤毛相关信号通路的调节。对 GLIS 信号通路上游的了解可能为开发糖尿病、甲状腺功能减退症和其他疾病的新治疗策略提供机会。

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