辅活化剂
PPARGC1A型
基因亚型
选择性拼接
生物
发起人
RNA剪接
过氧化物酶体增殖物激活受体
细胞生物学
基因
遗传学
转录因子
基因表达
核糖核酸
作者
Vicente Martínez-Redondo,Amanda Pettersson,Jorge L. Ruas
出处
期刊:Diabetologia
[Springer Nature]
日期:2015-06-25
卷期号:58 (9): 1969-1977
被引量:157
标识
DOI:10.1007/s00125-015-3671-z
摘要
Proteins of the peroxisome proliferator-activated receptor γ (PPARγ) coactivator 1 (PGC-1) family of transcriptional coactivators coordinate physiological adaptations in many tissues, usually in response to demands for higher nutrient and energy supply. Of the founding members of the family, PGC-1α (also known as PPARGC1A) is the most highly regulated gene, using multiple promoters and alternative splicing to produce a growing number of coactivator variants. PGC-1α promoters are selectively active in distinct tissues in response to specific stimuli. To date, more than ten novel PGC-1α isoforms have been reported to be expressed from a novel promoter (PGC-1α-b, PGC-1α-c), to undergo alternative splicing (NT-PGC-1α) or both (PGC-1α2, PGC-1α3, PGC-1α4). The resulting proteins display differential regulation and tissue distribution and, most importantly, exert specific biological functions. In this review we discuss the structural and functional characteristics of the novel PGC-1α isoforms, aiming to provide an integrative view of this constantly expanding system of transcriptional coactivators.
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