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核小体核心与真核生物转录起源于古菌的平行关系

Parallel origins of the nucleosome core and eukaryotic transcription from Archaea.

作者信息

Ouzounis C A, Kyrpides N C

机构信息

EMBL Heidelberg, Germany.

出版信息

J Mol Evol. 1996 Feb;42(2):234-9. doi: 10.1007/BF02198849.

Abstract

Computational sequence analysis of 10 available archaean histone-like proteins has shown that this family is not only divergently related to the eukaryotic core histones H2A/B, H3, and H4, but also to the central domain of subunits A and C of the CCAAT-binding factor (CBF), a transcription factor associated with eukaryotic promoters. Despite the low sequence identity, it is unambiguously shown that the core histone fold shares a common evolutionary history. Archaean histones and the two CBF families show a remarkable variability in contrast to eukaryotic core histones. Conserved residues shared between families are identified, possibly being responsible for the functional versatility of the core histone fold. The H4 subfamily is most similar to archaean proteins and may be the progenitor of the other core histones in eukaryotes. While it is not clear whether archaean histones are more actively involved in transcription regulation, the present observations link two processes, nucleosomal packing and transcription in a unique way. Both these processes, evidently hybrid in Archaea, have originated before the ermergence of the eukaryotic cell.

摘要

对10种可用的古菌组蛋白样蛋白进行的计算序列分析表明,该家族不仅与真核核心组蛋白H2A/B、H3和H4存在远缘关系,而且与CCAAT结合因子(CBF)的A和C亚基的中央结构域也有关系,CBF是一种与真核启动子相关的转录因子。尽管序列同一性较低,但明确表明核心组蛋白折叠具有共同的进化历史。与真核核心组蛋白相比,古菌组蛋白和两个CBF家族表现出显著的变异性。确定了家族之间共享的保守残基,这些残基可能是核心组蛋白折叠功能多样性的原因。H4亚家族与古菌蛋白最相似,可能是真核生物中其他核心组蛋白的祖先。虽然尚不清楚古菌组蛋白是否更积极地参与转录调控,但目前的观察结果以独特的方式将核小体组装和转录这两个过程联系起来。这两个过程在古菌中显然是混合的,它们起源于真核细胞出现之前。

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