大麦Hor2基因座的脉冲场凝胶电泳定位。

M B Sørensen
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引用次数: 21

摘要

用稀有切切限制性内切酶对原生质体释放的高分子量DNA进行酶切和脉冲场凝胶电泳分离。未消化DNA的平均大小在1500kbp以上。用NotI、SfiL、Mlul和SalI制作的酶切片段与编码B-hordein多肽的Hor2位点的所有基因杂交,发现该位点的最大大小为360 kbp。两个针对单个B-hordein基因的探针可以在位点上鉴定出两个片段类,每个片段类含有相同数量的B-hordein基因。双文摘可以对位点进行排序,并构建一个覆盖Hor2位点周围650 kbp的地图。没有证据表明这两个片段类有物理联系。讨论了这两类杂化片段可能归属于B1-和B3-hordein亚群。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mapping of the Hor2 locus in barley by pulsed field gel electrophoresis.

High molecular weight DNA released from isolated protoplasts was digested with rare-cutting restriction enzymes and separated by pulsed field gel electrophoresis. The average size of undigested DNA was above 1500 kbp. Digests made with NotI, SfiL, Mlul and SalI was hybridized to a probe, common to all genes of the Hor2 locus encoding B-hordein polypeptides, and this revealed the maximum size of the locus to be 360 kbp. Two probes, specific for individual B-hordein genes, enabled the identification of two fragment classes in the locus, each containing an equal number of B-hordein genes. Double digests allowed ordering of sites and construction of a map covering 650 kbp around the Hor2 locus. No evidence for physical linkage of the two fragment classes was obtained. The possible assignment of the two classes of hybridizing fragments to the B1- and B3-hordein subgroups is discussed.

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