Suppr超能文献

通过原位杂交对蝾螈灯刷染色体中组蛋白基因转录本进行定位

Localization of histone gene transcripts in newt lampbrush chromosomes by in situ hybridization.

作者信息

Old R W, Callan G H, Gross K W

出版信息

J Cell Sci. 1977;27:57-79. doi: 10.1242/jcs.27.1.57.

Abstract

Denatured 3H-labelled DNAs containing histone gene sequences originating from the echinoderms Psammechinus miliaris, Echimus esculentus and Strongylocentrotus purpuratus have been in situ hybridized to RNA transcripts on newt lampbrush chromosomes. Autoradiographs of the hybridized lampbrush preparations show labelling restricted to four or fewer lateral loop pairs all lying within the heteromorphic regions of chromosome I, also one or two loop pairs on chromosome VI, one loop pair on chromosome X and one loop pair on chromosome XI. For oocytes from a single newt, coincident label distribution is found with DNA's of diverse echinoderm origin; however different newts show some specific individual diversity in label distribution, including heterozygosity in the case of loops on bivalents VI and X. The more conspicuously labelled loops, particularly those on chromosome I, show a pattern of labelling which is explicable if the newt histone DNA sequences are confined to short intercepts of lateral loop axis. Transcription is initiated prior to the histone DNA sequences, proceeds through the histone DNA sequences, and beyond, and the histone RNA sequences are cut from the transcripts before the termination of transcription.

摘要

含有源自海胆(Psammechinus miliaris、Echimus esculentus和Strongylocentrotus purpuratus)的组蛋白基因序列的变性3H标记DNA,已与蝾螈灯刷染色体上的RNA转录本进行原位杂交。杂交灯刷制剂的放射自显影片显示,标记仅限于四个或更少的侧环对,它们都位于I号染色体的异形区域内,还有VI号染色体上的一两个环对、X号染色体上的一个环对和XI号染色体上的一个环对。对于来自单个蝾螈的卵母细胞,发现不同海胆来源的DNA具有一致的标记分布;然而,不同的蝾螈在标记分布上表现出一些特定的个体差异,包括VI号和X号二价体上的环的杂合性。标记更明显的环,特别是I号染色体上的那些环,显示出一种标记模式,如果蝾螈组蛋白DNA序列局限于侧环轴的短截段,这种模式是可以解释的。转录在组蛋白DNA序列之前启动,通过组蛋白DNA序列并继续进行,并且组蛋白RNA序列在转录终止之前从转录本中切割下来。

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