Gottlob-McHugh S G, Lévesque M, MacKenzie K, Olson M, Yarosh O, Johnson D A
Department of Biology, University of Ottawa, Ont., Canada.
Genome. 1990 Aug;33(4):486-94. doi: 10.1139/g90-072.
The 5S rRNA gene of the soybean Glycine max (L.) Merr. has been cloned on a 556-bp fragment of DNA and sequenced. This fragment contains two copies of the soybean 5S rDNA sequence, one intact and one truncated, separated by noncoding DNA. We have used this clone to investigate the organization of the 5S genes within the soybean genome and the extent of their methylation. Our results demonstrate that soybean 5S genes are clustered, organized into tandem repeats of 330 bp, and extensively methylated. Hybridization of the 5S sequence to Southern transfers of soybean DNA digested with BamHI reveals a striking ladderlike pattern. Hybridization of the soybean 5S sequence to a wide variety of plant DNAs results in similar patterns, suggesting that the 5S rDNA sequence, gene organization, and methylation pattern are conserved in many higher plants.
大豆(Glycine max (L.) Merr.)的5S rRNA基因已被克隆到一段556 bp的DNA片段上并进行了测序。该片段包含两个大豆5S rDNA序列拷贝,一个完整,一个截短,由非编码DNA隔开。我们利用这个克隆来研究大豆基因组中5S基因的组织方式及其甲基化程度。我们的结果表明,大豆5S基因成簇存在,组织成330 bp的串联重复序列,并且甲基化程度很高。5S序列与用BamHI消化的大豆DNA的Southern转移杂交显示出显著的梯状模式。大豆5S序列与多种植物DNA杂交产生相似的模式,这表明5S rDNA序列、基因组织方式和甲基化模式在许多高等植物中是保守的。