...
首页> 外文期刊>Plant physiology >Analysis of the molecular basis of flowering time variation in Arabidopsis accessions
【24h】

Analysis of the molecular basis of flowering time variation in Arabidopsis accessions

机译:拟南芥种开花时间变化的分子基础分析

获取原文
获取原文并翻译 | 示例
           

摘要

Allelic variation at the FRI (FRIGIDA) and FLC (FLOWERING LOCUS C) loci are major determinants of flowering time in Arabidopsis accessions. Dominant alleles of FRI confer a vernalization requirement causing plants to overwinter vegetatively. Many early flowering accessions carry loss-of-function fri alleles containing one of two deletions. However, some accessions categorized as early flowering types do not carry these deletion alleles. We have analyzed the molecular basis of earliness in five of these accessions: Cvi, Shakhdara, Wil-2, Kondara, and Kz-9. The Cvi FRI allele carries a number of nucleotide differences, one of which causes an in-frame stop codon in the first exon. The other four accessions contain nucleotide differences that only result in amino acid substitutions. Preliminary genetic analysis was consistent with Cvi carrying a nonfunctional FRI allele; Wil-2 carrying either a defective FRI or a dominant suppressor of FRI function; and Shakhdara, Kondara, and Kz-9 carrying a functional FRI allele with earliness being caused by allelic variation at other loci including FLC. Allelic variation at FLC was also investigated in a range of accessions. A novel nonautonomous Mutator-like transposon was found in the weak FLC allele in Landsberg erecta, positioned in the first intron, a region required for normal FLC regulation. This transposon was not present in FLC alleles of most other accessions including Shakhdara, Kondara, or Kz-9. Thus, variation in Arabidopsis flowering time has arisen through the generation of nonfunctional or weak FRI and FLC alleles.
机译:FRI(FRIGIDA)和FLC(FLOWERING LOCUS C)位点的等位基因变异是拟南芥种中开花时间的主要决定因素。 FRI的优势等位基因赋予了春化要求,导致植物无营养越冬。许多早期开花物带有功能缺失的等位基因,其中包含两个缺失之一。但是,一些归类为早期开花类型的种质没有携带这些缺失等位基因。我们已经分析了其中五个种的早期性的分子基础:Cvi,Shakhdara,Wil-2,Kondad和Kz-9。 Cvi FRI等位基因带有许多核苷酸差异,其中一个会在第一个外显子中引起读框内终止密码子。其他四个部分包含核苷酸差异,仅导致氨基酸取代。初步基因分析与携带无功能FRI等位基因的Cvi一致。 Wil-2携带有缺陷的FRI或FRI功能的主要抑制因子; Shakhdara,Kondara和Kz-9携带功能性FRI等位基因,且早期是由其他位点(包括FLC)的等位基因变异引起的。还研究了FLC等位基因变异的范围。在位于第一内含子(正常FLC调节所需的区域)中的Landsberg erecta的弱FLC等位基因中发现了一种新型的非自发突变体样转座子。该转座子在包括Shakhdara,Kondara或Kz-9在内的大多数其他种质的FLC等位基因中不存在。因此,拟南芥开花时间的变化已经通过产生无功能的或弱的FRI和FLC等位基因而产生。

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