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大豆 18S 和 25S 核糖体 RNA 基因的纯化和限制内切酶图谱。

Purification and restriction endonuclease mapping of soybean 18 S and 25 S ribosomal RNA genes.

机构信息

Lehrstuhl für Genetik, Institut für Biologie II der Universität, Auf der Morgenstelle 28, D-7400, Tübingen, Federal Republic of Germany.

出版信息

Planta. 1979 Sep;146(4):467-73. doi: 10.1007/BF00380862.

Abstract

The restriction endonuclease map of the 25 S and 18 S ribosomal RNA genes of a higher plant is presented. Soybean (Glycine max) rDNA was enriched by preparative buoyant density centrifugation in CsCl-actinomycin D gradients. The buoyant density of the rDNA was determined to be 1.6988 g cm(-3) by analytical centrifugation in CsCl. Saturation hybridization showed that 0.1% of the total DNA contains 25 S and 18 S rRNA coding sequences. This is equivalent to 800 rRNA genes per haploid genome (DNA content: 1.29 pg) or 3200 for the tetraploid genome. Restriction endonuclease mapping was performed with Bam H I, Hind III, Eco R I, and BstI. The repeating unit of the soybean ribosomal DNA has a molecular weight of 5.9·10(6) or approximately 9,000 kb. The 25 S and 18 S rRNA coding sequences were localized within the restriction map of the repeating unit by specific hybridization with either [(125)I]25 S or [(125)I]18 S rRNA. It was demonstrated that there is no heterogeneity even in the spacer region of the soybean rDNA.

摘要

呈现了一种高等植物 25S 和 18S 核糖体 RNA 基因的限制内切酶图谱。通过 CsCl-放线菌素 D 梯度的制备性浮力密度离心来富集大豆(Glycine max)rDNA。通过 CsCl 中的分析离心确定 rDNA 的浮力密度为 1.6988 g cm(-3)。饱和杂交表明,总 DNA 的 0.1% 含有 25S 和 18S rRNA 编码序列。这相当于每个单倍体基因组(DNA 含量:1.29 pg)有 800 个 rRNA 基因,或四倍体基因组有 3200 个。用 Bam H I、Hind III、Eco R I 和 BstI 进行了限制内切酶作图。大豆核糖体 DNA 的重复单元分子量为 5.9·10(6)或约 9000 kb。通过用 [(125)I]25S 或 [(125)I]18S rRNA 进行特异性杂交,将 25S 和 18S rRNA 编码序列定位在重复单元的限制图谱内。证明了即使在大豆 rDNA 的间隔区也没有异质性。

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