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花旗松5S rRNA基因的物理图谱构建与特征分析

Physical mapping and characterization of 5S rRNA genes in Douglas-fir.

作者信息

Amarasinghe V, Carlson J E

机构信息

Biotechnology Laboratory, University of British Columbia, Vancouver, Canada.

出版信息

J Hered. 1998 Nov-Dec;89(6):495-500. doi: 10.1093/jhered/89.6.495.

Abstract

Douglas-fir [Pseudotsuga menziesii (Mirb.) Franco] is one of the world's most valuable timber species and is widely used in reforestation. Therefore there is considerable interest in understanding its genetic structure. In conifers approximately 75% of the genome is composed of repetitive DNA. Thus for conifers characterization of repetitive DNA is a significant part of genome analysis. We have characterized the organization of 5S rRNA genes in Douglas-fir at both the molecular and chromosome levels. 5S DNA repeat units containing the coding sequence for 5S rRNA and the nontranscribed spacer (NTS) were cloned using PCR. Sequencing and Southern hybridization revealed repeat units of 888 and 871 bp in length, the latter with a 17 bp deletion in the NTS. The coding region showed high homology with other eukaryotic 5S rRNA genes. A 35 bp region of the NTS immediately upstream of the 5' end of the coding region showed high similarity to other conifers but not to other published plant 5S rDNA sequences. Physical mapping of 5S rDNA by fluorescent in situ hybridization using a biotinilated homologous probe revealed a single subtelomeric site on one pair of large metacentric chromosomes.

摘要

花旗松[北美黄杉(Pseudotsuga menziesii (Mirb.) Franco)]是世界上最具价值的木材树种之一,广泛用于植树造林。因此,人们对了解其遗传结构有着浓厚的兴趣。在针叶树中,约75%的基因组由重复DNA组成。因此,对针叶树而言,重复DNA的特征分析是基因组分析的重要组成部分。我们已在分子和染色体水平上对花旗松5S rRNA基因的组织进行了特征分析。利用PCR克隆了包含5S rRNA编码序列和非转录间隔区(NTS)的5S DNA重复单元。测序和Southern杂交显示重复单元长度分别为888 bp和871 bp,后者的NTS中有一个17 bp的缺失。编码区与其他真核生物5S rRNA基因具有高度同源性。编码区5'端上游紧邻的NTS的一个35 bp区域与其他针叶树具有高度相似性,但与其他已发表的植物5S rDNA序列不同。使用生物素化的同源探针通过荧光原位杂交对5S rDNA进行物理定位,结果显示在一对大型中着丝粒染色体上有一个单一的亚端粒位点。

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