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核糖体基因特异性转录因子的锌指结构

Zinc finger structure of a ribosomal gene-specific transcription factor.

作者信息

Hanas J S, Littell R M, Gaskins C J, Zebrowski R

机构信息

Department of Biochemistry and Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City 73190.

出版信息

SAAS Bull Biochem Biotechnol. 1990 Jan;3:85-90.

PMID:1367425
Abstract

Xenopus transcription factor IIIA (TFIIIA) or TFIIIA mutants with internal deletions were expressed in E.coli, isolated from E.coli cell extracts, and identified by SDS PAGE and immunoblotting with rabbit antiserum against native TFIIIA. Specific DNA binding of intact or internally deleted TFIIIA was compared by analyzing their abilities to protect the internal control region (ICR) of the Xenopus 5S ribosomal RNA gene from DNase I digestion. Intact protein bound specifically to the entire ICR (+96 to +43). One TFIIIA deletion mutant, expressed from cDNA lacking the coding sequence for the putative fourth zinc finger protected the ICR from DNase I digestion from nucleotide positions +96 to +78. A second TFIIIA mutant resulting from fusion of putative zinc fingers 7 and 8 protected the 5S gene ICR from positions +96 to +63. The regions of the protein comprising the N-terminal 3 fingers and N-terminal six fingers appear to be in contact with approximately 18 and 33 bp of DNA respectively on the 3' side of the 5S gene ICR.

摘要

非洲爪蟾转录因子IIIA(TFIIIA)或具有内部缺失的TFIIIA突变体在大肠杆菌中表达,从大肠杆菌细胞提取物中分离出来,并通过SDS-PAGE和用针对天然TFIIIA的兔抗血清进行免疫印迹鉴定。通过分析完整或内部缺失的TFIIIA保护非洲爪蟾5S核糖体RNA基因的内部控制区(ICR)免受DNase I消化的能力,比较了它们与特异性DNA的结合情况。完整的蛋白质特异性结合整个ICR(+96至+43)。一种从缺少假定的第四个锌指编码序列的cDNA表达的TFIIIA缺失突变体保护ICR免受从核苷酸位置+96至+78的DNase I消化。由假定的锌指7和8融合产生的第二个TFIIIA突变体保护5S基因ICR从位置+96至+63。包含N端3个锌指和N端6个锌指的蛋白质区域似乎分别与5S基因ICR 3'侧约18和33 bp的DNA接触。

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