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着丝粒相关DNA中的支架附着区域。

Scaffold attachment regions in centromere-associated DNA.

作者信息

Strissel P L, Espinosa R, Rowley J D, Swift H

机构信息

Department of Hematology/Oncology, University of Chicago, Chicago, IL 60637, USA.

出版信息

Chromosoma. 1996 Aug;105(2):122-33. doi: 10.1007/BF02509522.

Abstract

Due to indications that kinetochore proteins are an integral part of the protein scaffold component of the chromosome (Earnshaw et al. 1984), we chose to map the distribution of scaffold attachment regions (SARs) at centromeres. Using the SAR mapping assay of Mirkovitch et al., Southern blots were prepared and probed with 32P-labeled fragments from the human 1.9 kb centromeric alpha-satellite repeat unit of chromosome 1 or the 1.7 kb centromeric alpha-satellite repeat unit of chromosome 16. Our results demonstrated the presence of one SAR site per 1.9 kb repeat unit in chromosome 1, and every 1.7 kb repeat unit in chromosome 16, separated by regions of small DNA loops over the length of the alpha-satellite regions. We also identified several in vitro vertebrate topoisomerase II and cenP-B consensus sequences throughout the chromosome 1 alpha-satellite region using computer and base ratio analysis, to address the question as to why some alpha-satellite regions are SAR related and others are not. To provide in situ indications of SAR localization in the human genome, SAR DNA and non-SAR DNA were prepared following lithium 3,5-di-iodosalicylate extraction. Sequences protected from DNAse I digestion by SAR proteins, as compared with unprotected DNA that was digested by the enzyme, was labeled with biotin-UTP, hybridized to chromosomal DNA in situ, and then detected with fluorescein-avidin-DCS. Both SAR and non-SAR DNA selectively labeled virtually all centromeric regions of the human metaphase karyotype. Chromosomal arms were less strongly bound by SAR DNA, with a pattern that followed the chromosomal axis. In the more condensed chromosomes an R-banding pattern was evident. In general, labeling patterns produced by both SAR and non-SAR fractions were similar, as expected from the indications that SAR DNAs are heterogenous in sequence and do not form a specific class of sequences. We conclude that centromeric regions of several, possibly all, human metaphase chromosomes are also regions where the chromosomal axis contains loops, smaller in size than in the arms and where attachment sites are concentrated. This clustering of SARs may be responsible in part for the tight chromatin packing associated with the primary constriction of the centromeric region.

摘要

由于有迹象表明动粒蛋白是染色体蛋白质支架成分的一个组成部分(厄恩肖等人,1984年),我们选择绘制着丝粒处支架附着区域(SARs)的分布图。使用米尔科维奇等人的SAR映射分析方法,制备了Southern印迹,并用人染色体1的1.9 kb着丝粒α卫星重复单元或染色体16的1.7 kb着丝粒α卫星重复单元的32P标记片段进行探测。我们的结果表明,染色体1中每1.9 kb重复单元存在一个SAR位点,染色体16中每1.7 kb重复单元存在一个SAR位点,在α卫星区域的长度上,这些位点被小DNA环区域隔开。我们还使用计算机和碱基比率分析,在整个染色体1的α卫星区域鉴定了几个体外脊椎动物拓扑异构酶II和着丝粒蛋白B共有序列,以解决为什么一些α卫星区域与SAR相关而其他区域不相关的问题。为了提供SAR在人类基因组中定位的原位指示,在3,5 - 二碘水杨酸锂提取后制备了SAR DNA和非SAR DNA。与被该酶消化的未受保护的DNA相比,被SAR蛋白保护免受DNA酶I消化的序列用生物素 - UTP标记,原位杂交到染色体DNA上,然后用荧光素 - 抗生物素蛋白 - DCS检测。SAR DNA和非SAR DNA都选择性地标记了人类中期核型的几乎所有着丝粒区域。染色体臂与SAR DNA的结合较弱,其模式沿着染色体轴。在更浓缩的染色体中,R带模式明显。一般来说,SAR和非SAR部分产生的标记模式相似,正如从SAR DNA序列异质且不形成特定序列类别的迹象所预期的那样。我们得出结论,几个,可能是所有,人类中期染色体的着丝粒区域也是染色体轴包含环的区域,但环的尺寸比染色体臂中的小,并且附着位点集中。SARs的这种聚集可能部分负责与着丝粒区域主要缢缩相关的紧密染色质包装。

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