核糖体基因特异性转录因子的锌指结构。

J S Hanas, R M Littell, C J Gaskins, R Zebrowski
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引用次数: 0

摘要

在大肠杆菌中表达爪蟾转录因子IIIA (TFIIIA)或内部缺失的TFIIIA突变体,从大肠杆菌细胞提取物中分离得到,用SDS PAGE和兔抗TFIIIA抗体进行免疫印迹鉴定。通过分析完整的TFIIIA和内部缺失的TFIIIA对爪蟾5S核糖体RNA基因内控区(ICR)免受DNA酶I酶切的保护能力,比较它们的特异性DNA结合。完整蛋白与整个ICR特异性结合(+96 ~ +43)。一个TFIIIA缺失突变体,由缺乏第四个锌指编码序列的cDNA表达,保护ICR免受DNase I从+96到+78核苷酸位置的消化。第二个TFIIIA突变体由推定的锌指7和8融合产生,保护5S基因ICR从+96位到+63位。包含n端3指和n端6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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Zinc finger structure of a ribosomal gene-specific transcription factor.

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.

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