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发现体内的敌人:Krüppel相关盒锌指蛋白家族对哺乳动物基因组中外源DNA的靶向沉默

Spotting the enemy within: Targeted silencing of foreign DNA in mammalian genomes by the Krüppel-associated box zinc finger protein family.

作者信息

Wolf Gernot, Greenberg David, Macfarlan Todd S

机构信息

The Eunice Kennedy Shriver National Institute of Child Health and Human Development, The National Institutes of Health, Bethesda, MD 20892 USA.

The Gladstone Institute of Virology and Immunology, University of California, San Francisco, CA 94158 USA ; Present address: Pacific Biosciences, 1380 Willow Road, Menlo Park, CA 94025 USA.

出版信息

Mob DNA. 2015 Oct 2;6:17. doi: 10.1186/s13100-015-0050-8. eCollection 2015.

Abstract

Tandem C2H2-type zinc finger proteins (ZFPs) constitute the largest transcription factor family in animals. Tandem-ZFPs bind DNA in a sequence-specific manner through arrays of multiple zinc finger domains that allow high flexibility and specificity in target recognition. In tetrapods, a large proportion of tandem-ZFPs contain Krüppel-associated-box (KRAB) repression domains, which are able to induce epigenetic silencing through the KAP1 corepressor. The KRAB-ZFP family continuously amplified in tetrapods through segmental gene duplications, often accompanied by deletions, duplications, and mutations of the zinc finger domains. As a result, tetrapod genomes contain unique sets of KRAB-ZFP genes, consisting of ancient and recently evolved family members. Although several hundred human and mouse KRAB-ZFPs have been identified or predicted, the biological functions of most KRAB-ZFP family members have gone unexplored. Furthermore, the evolutionary forces driving the extraordinary KRAB-ZFP expansion and diversification have remained mysterious for decades. In this review, we highlight recent studies that associate KRAB-ZFPs with the repression of parasitic DNA elements in the mammalian germ line and discuss the hypothesis that the KRAB-ZFP family primarily evolved as an adaptive genomic surveillance system against foreign DNA. Finally, we comment on the computational, genetic, and biochemical challenges of studying KRAB-ZFPs and attempt to predict how these challenges may be soon overcome.

摘要

串联C2H2型锌指蛋白(ZFPs)构成了动物中最大的转录因子家族。串联锌指蛋白通过多个锌指结构域阵列以序列特异性方式结合DNA,这使得在靶标识别中具有高度的灵活性和特异性。在四足动物中,很大一部分串联锌指蛋白含有Krüppel相关框(KRAB)抑制结构域,这些结构域能够通过KAP1共抑制因子诱导表观遗传沉默。KRAB-ZFP家族在四足动物中通过片段基因复制不断扩增,通常伴随着锌指结构域的缺失、重复和突变。因此,四足动物基因组包含独特的KRAB-ZFP基因集,由古老的和最近进化的家族成员组成。尽管已经鉴定或预测了数百种人类和小鼠的KRAB-ZFP,但大多数KRAB-ZFP家族成员的生物学功能仍未被探索。此外,几十年来,驱动KRAB-ZFP异常扩增和多样化的进化力量一直是个谜。在这篇综述中,我们重点介绍了最近将KRAB-ZFP与哺乳动物生殖系中寄生DNA元件的抑制联系起来的研究,并讨论了KRAB-ZFP家族主要作为一种针对外来DNA的适应性基因组监测系统进化而来的假说。最后,我们评论了研究KRAB-ZFP的计算、遗传和生化挑战,并试图预测这些挑战可能很快如何被克服。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5fa/4592553/78cd0ac461a4/13100_2015_50_Fig1_HTML.jpg

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