...
首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >A tandem duplication causes the Kn1-O allele of Knotted, a dominant morphological mutant of maize.
【24h】

A tandem duplication causes the Kn1-O allele of Knotted, a dominant morphological mutant of maize.

机译:串联重复导致Knotted的Kn1-O等位基因,Knotted是玉米的主要形态突变体。

获取原文
           

摘要

Molecular and genetic techniques are used to define Kn1-O, a mutation which interferes with the normal differentiation of vascular tissue in leaves. Sequences associated with a previously cloned allele, Kn1-2F11, were used as hybridization probes in a Southern analysis of Kn1-O. By this analysis, Kn1-O lacks the Ds2 transposable element that causes Kn1-2F11 but instead is associated with a sequence duplication. Sequence and restriction analysis of genomic clones show that the duplication consists of a tandem array of two 17-kb repeats. Analysis of Kn1-O derivatives indicates that the duplication itself conditions the mutant phenotype; a severely knotted line, Kn1-Ox, has gained a repeat unit to form a triplication, whereas normal derivatives have either lost a repeat unit or sustained insertions that disrupt the tandem duplication. These insertions map near the central junction of the tandem duplication, suggesting that the mutant phenotype results from the novel juxtaposition of sequences. We discuss models that relate the tandem duplication of sequences to altered gene expression.
机译:分子和遗传技术被用于定义Kn1-O,这是一种干扰叶片中维管组织正常分化的突变。与先前克隆的等位基因Kn1-2F11相关的序列在Kn1-O的Southern分析中用作杂交探针。通过该分析,Kn1-O缺乏导致Kn1-2F11的Ds2转座因子,但与序列重复相关。基因组克隆的序列和限制性分析表明,重复序列由两个17kb重复序列组成。对Kn1-O衍生物的分析表明,重复本身决定了突变体的表型。一个严重打结的线Kn1-Ox已获得一个重复单元以形成三联体,而正常的导数要么丢失了一个重复单元,要么连续插入而破坏了串联重复。这些插入定位在串联重复的中央连接附近,表明突变体表型是由新的并列序列产生的。我们讨论了将序列的串联重复与改变的基因表达相关的模型。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号