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哺乳动物核糖体基因终止子序列与转录终止因子TTF-I的分子协同进化

Molecular coevolution of mammalian ribosomal gene terminator sequences and the transcription termination factor TTF-I.

作者信息

Evers R, Grummt I

机构信息

Division of Molecular Biology of the Cell II, German Cancer Research Center, Heidelberg.

出版信息

Proc Natl Acad Sci U S A. 1995 Jun 20;92(13):5827-31. doi: 10.1073/pnas.92.13.5827.

Abstract

Both the DNA elements and the nuclear factors that direct termination of ribosomal gene transcription exhibit species-specific differences. Even between mammals--e.g., human and mouse--the termination signals are not identical and the respective transcription termination factors (TTFs) which bind to the terminator sequence are not fully interchangeable. To elucidate the molecular basis for this species-specificity, we have cloned TTF-I from human and mouse cells and compared their structural and functional properties. Recombinant TTF-I exhibits species-specific DNA binding and terminates transcription both in cell-free transcription assays and in transfection experiments. Chimeric constructs of mouse TTF-I and human TTF-I reveal that the major determinant for species-specific DNA binding resides within the C terminus of TTF-I. Replacing 31 C-terminal amino acids of mouse TTF-I with the homologous human sequences relaxes the DNA-binding specificity and, as a consequence, allows the chimeric factor to bind the human terminator sequence and to specifically stop rDNA transcription.

摘要

指导核糖体基因转录终止的DNA元件和核因子均表现出物种特异性差异。即使在哺乳动物之间,例如人类和小鼠,终止信号也不相同,并且与终止子序列结合的各自转录终止因子(TTF)也不能完全互换。为了阐明这种物种特异性的分子基础,我们从人类和小鼠细胞中克隆了TTF-I,并比较了它们的结构和功能特性。重组TTF-I表现出物种特异性DNA结合,并在无细胞转录测定和转染实验中终止转录。小鼠TTF-I和人类TTF-I的嵌合构建体表明,物种特异性DNA结合的主要决定因素位于TTF-I的C末端内。用同源人类序列替换小鼠TTF-I的31个C末端氨基酸可放宽DNA结合特异性,结果使嵌合因子能够结合人类终止子序列并特异性地停止rDNA转录。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b990/41594/79281987e970/pnas01489-0077-a.jpg

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