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利用脉冲场凝胶电泳对大麦中Hor2基因座进行定位。

Mapping of the Hor2 locus in barley by pulsed field gel electrophoresis.

作者信息

Sørensen M B

机构信息

Department of Physiology, Carlsberg Laboratory, Copenhagen Valby.

出版信息

Carlsberg Res Commun. 1989;54(3):109-20. doi: 10.1007/BF02908303.

Abstract

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.

摘要

从分离的原生质体中释放出的高分子量DNA用稀有切割限制酶进行消化,并用脉冲场凝胶电泳进行分离。未消化DNA的平均大小超过1500千碱基对。用NotI、SfiL、Mlul和SalI进行的消化产物与一个探针杂交,该探针与编码β-大麦醇溶蛋白多肽的Hor2基因座的所有基因共有,这表明该基因座的最大大小为360千碱基对。两个针对单个β-大麦醇溶蛋白基因的探针能够识别该基因座中的两类片段,每类片段包含相等数量的β-大麦醇溶蛋白基因。双酶切允许确定位点顺序并构建一个覆盖Hor2基因座周围650千碱基对的图谱。未获得两类片段存在物理连锁的证据。讨论了两类杂交片段与B1-和B3-大麦醇溶蛋白亚组的可能归属。

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