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人类核糖体RNA基因簇:包含新型串联重复序列的近端的鉴定。

Human ribosomal RNA gene cluster: identification of the proximal end containing a novel tandem repeat sequence.

作者信息

Sakai K, Ohta T, Minoshima S, Kudoh J, Wang Y, de Jong P J, Shimizu N

机构信息

Department of Molecular Biology, Keio University School of Medicine, Tokyo, Japan.

出版信息

Genomics. 1995 Apr 10;26(3):521-6. doi: 10.1016/0888-7543(95)80170-q.

Abstract

Human ribosomal RNA genes (rDNA) are arranged as tandem repeat clusters on the short arms of five pairs of acrocentric chromosomes. We have demonstrated that a majority of the rDNA clusters are detected as 3-Mb DNA fragments when released from human genomic DNA by EcoRV digestion. This indicated the absence of the EcoRV restriction site within the rDNA clusters. We then screened for rDNA-positive cosmid clones using a chromosome 22-specific cosmid library that was constructed from MboI partial digests of the flow-sorted chromosomes. Three hundred twenty rDNA-positive clones negative for the previously reported distal flanking sequence (pACR1) were chosen and subjected to EcoRV digestion. Seven clones susceptible to EcoRV were further characterized as candidate clones that might have been derived from the junctions of the 3-Mb rDNA cluster. We identified one clone containing part of the rDNA unit sequence and a novel flanking sequence. Detailed analysis of this unique clone revealed that the coding region of the last rRNA gene located at the proximal end of the cluster is interrupted with a novel sequence of approximately 147 bp that is tandemly repeated and is connected with an intervening 68-bp unique sequence. This junction sequence was readily amplified from chromosomes 21 and 15 as well as 22 using the polymerase chain reaction. Fluorescence in situ hybridization further indicated that the approximately 147-bp sequence repeat is commonly distributed among all the acrocentric short arms.

摘要

人类核糖体RNA基因(rDNA)在五对近端着丝粒染色体的短臂上排列成串联重复簇。我们已经证明,当通过EcoRV消化从人类基因组DNA中释放出来时,大多数rDNA簇被检测为3-Mb的DNA片段。这表明rDNA簇内不存在EcoRV限制位点。然后,我们使用从流式分选染色体的MboI部分消化构建的22号染色体特异性粘粒文库筛选rDNA阳性粘粒克隆。选择了320个对先前报道的远端侧翼序列(pACR1)呈阴性的rDNA阳性克隆,并进行EcoRV消化。七个对EcoRV敏感的克隆被进一步鉴定为可能源自3-Mb rDNA簇连接处的候选克隆。我们鉴定出一个包含部分rDNA单位序列和一个新的侧翼序列的克隆。对这个独特克隆的详细分析表明,位于簇近端的最后一个rRNA基因的编码区被一个约147 bp的新序列中断,该序列串联重复,并与一个68 bp的间隔独特序列相连。使用聚合酶链反应很容易从21号和15号以及22号染色体上扩增出这个连接序列。荧光原位杂交进一步表明,约147 bp的序列重复在所有近端着丝粒短臂中普遍分布。

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