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五核苷酸ATTGG,即“反向CCAAT”,是HLA I类基因转录的必需元件。

The pentanucleotide ATTGG, the "inverted CCAAT," is an essential element for HLA class I gene transcription.

作者信息

Schoneich J, Lee J L, Mansky P, Sheffery M, Yang S Y

机构信息

Immunology Program, Sloan-Kettering Institute for Cancer Research, New York, NY 10021, USA.

出版信息

J Immunol. 1997 May 15;158(10):4788-96.

PMID:9144493
Abstract

The HLA class I genes, HLA-A, -B, and -C, contain an inverted CCAAT sequence (ATTGG) located 20 bp upstream of the canonical CCAAT and approximately 70 bp upstream of the transcription initiation site. We have investigated the transcriptional function of the class I inverted CCAAT sequence using the HLA-normal cell line, HeLa. Deletion, mutation, or inversion of the inverted CCAAT sequence abrogated or reduced the activity of the class I promoter, as assessed by luciferase reporter gene assays in transient gene expression experiments. This activity coincided with occupancy of the inverted CCAAT motif, as tested by electrophoretic mobility shift assays using the wild-type sequence and mutated variants of the sequence. The ATTGG-binding protein was not CP2, NF-1, or other known CCAAT-binding proteins, but the complex may contain a CP1/NF-Y-like protein. Our results indicate that this inverted CCAAT sequence is an essential element for the expression of HLA class I genes and that its transcriptional activity depends upon the sequence, position, and orientation of the pentanucleotide.

摘要

HLA I类基因,即HLA - A、- B和- C,在典型CCAAT序列上游20 bp以及转录起始位点上游约70 bp处含有一个反向CCAAT序列(ATTGG)。我们利用HLA正常细胞系HeLa研究了I类反向CCAAT序列的转录功能。在瞬时基因表达实验中,通过荧光素酶报告基因检测评估,反向CCAAT序列的缺失、突变或倒置均消除或降低了I类启动子的活性。如使用野生型序列及其突变变体进行电泳迁移率变动分析所测试的那样,这种活性与反向CCAAT基序的占据情况一致。与ATTGG结合的蛋白不是CP2、NF - 1或其他已知的CCAAT结合蛋白,但该复合物可能包含一种CP1/NF - Y样蛋白。我们的结果表明,这种反向CCAAT序列是HLA I类基因表达的必需元件,其转录活性取决于五核苷酸的序列、位置和方向。

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