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含KRAB结构域的锌指蛋白的进化及其在物种进化中的作用。

Evolution of KRAB-containing zinc finger proteins and their roles in species evolution.

作者信息

Wang Jin-long, Wang Jian, Tian Chun-yan

机构信息

State Key Laboratory of Proteomics, National Center for Proteomics Science (Beijing), China National Engineering Research Center for Protein Drugs, Beijing Institute of Radiation Medicine, Beijing 102206, China.

出版信息

Yi Chuan. 2016 Nov 20;38(11):971-978. doi: 10.16288/j.yczz.16-056.

DOI:10.16288/j.yczz.16-056
PMID:27867147
Abstract

The C2H2 zinc finger protein family, one of the largest families of transcription factor/transcriptional regulator in mammal, arose from a small ancestral group of eukaryotic zinc finger transcription factors through many repeated gene duplications accompanied by functional divergence. As the biggest subfamily of C2H2 zinc finger protein family, Kruppel-associated box-containing zinc finger proteins (KRAB-ZFPs) appeared at the period oftetrapod, expand rapidly along with species evolution, and take about 60% of the total C2H2 zinc finger proteins in human. During species evolution, the DNA binding ability of KRAB-ZFPs is changed while the KRAB-ZFPs-mediate transcriptional repression ability maintains stable under the evolution pressure. Moreover, multiple KRAB-ZFPs function synergistically with KAP1 on transcriptional silencing of retroelements, and the coevolution between KRAB-ZFPs and target retrotransposons restrict the jumping ability of the retroelements. In this review, we summarize the roles of KRAB-ZFPs duplication, the flexibility of zinc finger structure, transcriptional repression of KRAB-ZFPs/KAP1 and retroelement "jump" in promoting the divergence in regulatory network, stable genome change and species evolution, in order to reveal the characters and functions of KRAB-ZFPs in driving species evolution stably.

摘要

C2H2锌指蛋白家族是哺乳动物中最大的转录因子/转录调节因子家族之一,它起源于一小群真核生物锌指转录因子,经过多次重复基因复制并伴随着功能分化。作为C2H2锌指蛋白家族中最大的亚家族,含克鲁ppel相关框的锌指蛋白(KRAB-ZFPs)出现在四足动物时期,随着物种进化迅速扩张,在人类中占C2H2锌指蛋白总数的约60%。在物种进化过程中,KRAB-ZFPs的DNA结合能力发生变化,而其介导的转录抑制能力在进化压力下保持稳定。此外,多个KRAB-ZFPs与KAP1在逆转录元件的转录沉默中协同发挥作用,KRAB-ZFPs与靶逆转录转座子之间的共同进化限制了逆转录元件的跳跃能力。在这篇综述中,我们总结了KRAB-ZFPs复制的作用、锌指结构的灵活性、KRAB-ZFPs/KAP1的转录抑制以及逆转录元件“跳跃”在促进调控网络分歧、稳定基因组变化和物种进化中的作用,以揭示KRAB-ZFPs在稳定推动物种进化中的特征和功能。

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