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鸡H3组蛋白基因同源对共享的5'侧翼区域中存在明显的转录调控元件。

Presence of distinct transcriptional regulatory elements in the 5'-flanking region shared by the chicken H3 histone gene homopair.

作者信息

Takami Y, Nakayama T

机构信息

Department of Biochemistry, Miyazaki Medical College, Japan.

出版信息

Nucleic Acids Res. 1992 Jun 25;20(12):3037-41. doi: 10.1093/nar/20.12.3037.

Abstract

The chicken H3 histone gene family contains nine members belonging to two major histone gene clusters. Six of these genes have been sequenced and shown to encode two different H3 protein variants. Five H3 genes (H3-I, -II, -IV, -V, and -VI) encode the same amino acid sequence (class I) and another H3 gene (H3-III) differs from class I in a single amino acid (IIe113-Met) (class II). H3-II and H3-III have inverted orientations and share a 5' intergenic region of about 900 bp. To understand the regulation of expression of these two genes, we fused the 5'-flanking region to the CAT gene in inverted orientations to generate two chimeric plasmids, pH3-II-900 and pH3-III-900. Transient CAT assays using these constructs indicated that the promoter of H3-III is more active than that of H3-II. CAT assays with deletion mutants showed that H3-II and H3-III each possess a particular transcription regulatory sequence 5' adjacent to their coding sequence. In addition, the functional sequences of H3-II have no effect on expression of H3-III and vice versa. These results suggest that the regulations of expression of the two H3 genes are distinct.

摘要

鸡H3组蛋白基因家族包含九个成员,分属于两个主要的组蛋白基因簇。其中六个基因已被测序,并显示编码两种不同的H3蛋白变体。五个H3基因(H3-I、-II、-IV、-V和-VI)编码相同的氨基酸序列(I类),另一个H3基因(H3-III)在单个氨基酸(Ile113-Met)上与I类不同(II类)。H3-II和H3-III具有反向取向,并共享约900 bp的5'基因间隔区。为了了解这两个基因的表达调控,我们将5'侧翼区以反向取向与CAT基因融合,以产生两个嵌合质粒,pH3-II-900和pH3-III-900。使用这些构建体进行的瞬时CAT分析表明,H3-III的启动子比H3-II的启动子更具活性。对缺失突变体进行的CAT分析表明,H3-II和H3-III在其编码序列相邻的5'端各自拥有一个特定的转录调控序列。此外,H3-II的功能序列对H3-III的表达没有影响,反之亦然。这些结果表明,这两个H3基因的表达调控是不同的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b339/312434/0e345255afda/nar00086-0110-a.jpg

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