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小麦中的5S核糖体基因簇:脉冲场凝胶电泳揭示了高度多态性。

5S ribosomal gene clusters in wheat: pulsed field gel electrophoresis reveals a high degree of polymorphism.

作者信息

Röder M S, Sorrells M E, Tanksley S D

机构信息

Department of Plant Breeding and Biometry, Cornell University, Ithaca, NY 14853.

出版信息

Mol Gen Genet. 1992 Mar;232(2):215-20. doi: 10.1007/BF00279999.

Abstract

The long-range structure of 5S rRNA gene clusters has been investigated in wheat (Triticum aestivum L.) by means of pulsed field gel electrophoresis. Using aneuploid stocks, 5S rRNA gene clusters were assigned to sites on chromosomes 1B, 1D, 5B and 5D. Cluster sizes were evaluated and the copy number of 5S DNA repeats was estimated at 4700-5200 copies for the short repeating unit (410 bp) and about 3100 copies for the long repeat (500 bp) per haploid genome. A comparison of wheat cultivars revealed extremely high levels of polymorphism in the 5S rRNA gene clusters. With one restriction enzyme digest all varieties tested gave unique banding patterns and, on a per fragment basis, 21-fold more polymorphism was detected among cultivars for 5S DNA compared to standard restriction fragment length polymorphisms (RFLPs) detected with single copy clones. Experiments with aneuploid stocks suggest that the 5S rRNA gene clusters at several chromosomal sites contribute to this polymorphism. A number of previous reports have shown that wheat cultivars are not easily distinguished by isozymes or RFLPs. The high level of variation detected in 5S rRNA gene clusters therefore offers the possibility of a sensitive fingerprinting method for wheat. 5S DNA and other macro-satellite sequences may also serve as hypervariable Mendelian markers for genetic and breeding experiments in wheat.

摘要

利用脉冲场凝胶电泳技术,对小麦(Triticum aestivum L.)5S rRNA基因簇的长程结构进行了研究。通过非整倍体系,将5S rRNA基因簇定位到1B、1D、5B和5D染色体上。评估了基因簇大小,并估计每个单倍体基因组中短重复单元(410 bp)的5S DNA重复拷贝数为4700 - 5200个,长重复单元(500 bp)约为3100个拷贝。对小麦品种的比较显示,5S rRNA基因簇中存在极高水平的多态性。用一种限制酶消化后,所有测试品种都呈现出独特的条带模式,并且在每个片段基础上,与单拷贝克隆检测到的标准限制性片段长度多态性(RFLP)相比,5S DNA在品种间检测到的多态性高21倍。非整倍体系实验表明,几个染色体位点上的5S rRNA基因簇促成了这种多态性。此前的许多报道表明,小麦品种不易通过同工酶或RFLP进行区分。因此,在5S rRNA基因簇中检测到的高水平变异为小麦提供了一种灵敏的指纹识别方法的可能性。5S DNA和其他大卫星序列也可作为小麦遗传和育种实验中的高变孟德尔标记。

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