Suppr超能文献

来自酿酒酵母的DNA连接酶基因(CDC9)的核苷酸序列:一个受细胞周期调控并在DNA损伤时被诱导的基因。

The nucleotide sequence of the DNA ligase gene (CDC9) from Saccharomyces cerevisiae: a gene which is cell-cycle regulated and induced in response to DNA damage.

作者信息

Barker D G, White J H, Johnston L H

出版信息

Nucleic Acids Res. 1985 Dec 9;13(23):8323-37. doi: 10.1093/nar/13.23.8323.

Abstract

The CDC9 gene of Saccharomyces cerevisiae encodes a DNA ligase, and we have determined the nucleotide sequence of a 3.85 kb fragment of DNA which encompasses the convergently transcribed CDC9 and CDC36 genes. S1 nuclease mapping has revealed a major 5' end for the CDC9 mRNA, and one major and one minor site for 3' polyadenylation. These two sites lie within the C-terminal coding region of the CDC36 gene, implying that these two genes are transcribed from overlapping sequences. An interesting structural feature of the CDC9 gene is a series of 6 hexanucleotide repeats (ATGATT) which occur within the 650 bp immediately upstream from the site of transcription initiation. These repeat elements may be implicated in the cell division cycle regulated expression of CDC9. Comparison of the predicted amino acid sequence of the yeast DNA ligase (Mr 84,806) with the sequences of the T4 and T7 bacteriophage DNA ligases reveals little similarity except for a stretch of approximately 45 amino acids, comprising 3 short homologous segments. This region may represent an ATP-binding domain common to polynucleotide ligases.

摘要

酿酒酵母的CDC9基因编码一种DNA连接酶,我们已经确定了一段3.85 kb DNA片段的核苷酸序列,该片段包含反向转录的CDC9和CDC36基因。S1核酸酶图谱分析揭示了CDC9 mRNA的一个主要5'末端,以及3'多聚腺苷酸化的一个主要位点和一个次要位点。这两个位点位于CDC36基因的C末端编码区内,这意味着这两个基因是从重叠序列转录而来的。CDC9基因一个有趣的结构特征是一系列6个六核苷酸重复序列(ATGATT),它们出现在转录起始位点上游650 bp内。这些重复元件可能与CDC9在细胞分裂周期调控的表达有关。将酵母DNA连接酶的预测氨基酸序列(Mr 84,806)与T4和T7噬菌体DNA连接酶的序列进行比较,发现除了一段约45个氨基酸组成的序列(包含3个短同源片段)外,几乎没有相似性。该区域可能代表多核苷酸连接酶共有的ATP结合结构域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ffc/322137/6dbeb5370894/nar00317-0047-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验