Suppr超能文献

酿酒酵母减数分裂特异性基因SPO13的核苷酸序列及启动子分析。

Nucleotide sequence and promoter analysis of SPO13, a meiosis-specific gene of Saccharomyces cerevisiae.

作者信息

Buckingham L E, Wang H T, Elder R T, McCarroll R M, Slater M R, Esposito R E

机构信息

Department of Molecular Genetics and Cell Biology, University of Chicago, IL 60637.

出版信息

Proc Natl Acad Sci U S A. 1990 Dec;87(23):9406-10. doi: 10.1073/pnas.87.23.9406.

Abstract

The SPO13 gene, required for meiosis I segregation in Saccharomyces cerevisiae, produces two developmentally regulated transcripts (1.0 and 1.4 kilobases) that differ in length at their 5' ends. The shorter transcript is sufficient to complement the spo13-1 mutation and contains a major open reading frame encoding a highly basic protein of 33.4 kilodaltons. A fragment upstream (-170 to -8) of the open reading frame confers meiosis-specific transcription on a spo13-HIS3 fusion. Deletions at the 5' end of spo13-lacZ fusions define a region between -140 and -80 that is essential for meiosis-specific expression. This region acts in an orientation-independent manner and is responsive to the MAT-RME regulatory cascade. It contains a 10-base-pair sequence, TAGCCGCCGA, found in a number of meiosis-specific genes, that appears to be required for SPO13 expression. This sequence is identical to URS1, a ubiquitous mitotic repressor element.

摘要

酿酒酵母减数分裂I分离所需的SPO13基因产生两种受发育调控的转录本(1.0和1.4千碱基),它们在5'端的长度不同。较短的转录本足以弥补spo13-1突变,并且包含一个主要的开放阅读框,编码一个33.4千道尔顿的高度碱性蛋白。开放阅读框上游(-170至-8)的一个片段赋予spo13-HIS3融合体减数分裂特异性转录。spo13-lacZ融合体5'端的缺失定义了一个-140至-80之间的区域,该区域对于减数分裂特异性表达至关重要。该区域以不依赖方向的方式起作用,并对MAT-RME调控级联反应有反应。它包含一个10碱基对序列TAGCCGCCGA,在许多减数分裂特异性基因中都有发现,似乎是SPO13表达所必需的。这个序列与URS1相同,URS1是一种普遍存在的有丝分裂抑制元件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dba/55174/7cdc53c9fdd8/pnas01048-0345-a.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验