| 注册
首页|期刊导航|棉花学报|陆地棉GhSPL3基因的克隆、亚细胞定位及表达分析

陆地棉GhSPL3基因的克隆、亚细胞定位及表达分析

李洁 范术丽 宋美珍 庞朝友 喻树迅

棉花学报2012,Vol.24Issue(5):414-419,6.
棉花学报2012,Vol.24Issue(5):414-419,6.

陆地棉GhSPL3基因的克隆、亚细胞定位及表达分析

Cloning,Subcellular Localization and Expression Analysis of GhSPL3 Gene in Gossypium hirsutum L

李洁 1范术丽 2宋美珍 2庞朝友 2喻树迅2

作者信息

  • 1. 西北农林科技大学,陕西杨凌712100
  • 2. 中国农业科学院棉花研究所/棉花生物学国家重点实验室,河南安阳455000
  • 折叠

摘要

Abstract

GhSPL3, an SPL transcription factor, was cloned from upland cotton by bioinformation and RT-PCR technology. The sequence accession number is JN795132 in GenBank. The ORF length of GhSPLi is 426 bp which encodes 141 amino acid residues. Bioinformatics analysis showed that GhSPLi contains a typical SBP structure domain and a nuclear localization signal; Evolutionary tree analysis revealed that GhSPLi and AtSPLi were clustered in same group, thus GhSPLi and AtSPLi might have similar structure and function. Subcellular localization results showed that the signal of GhSPLi was localized in the nucleus. Quantitative RT-PCR results showed that GhSPLi expressed in all tissues, but the expression levels were different. The expression of GhSPLi in the flowers was the highest, and the lower was that in shoot apexes and in stem, followed by that in the root and in the leaves. Among different development stages of shoot apex, the expression of GhSPLi was the highest at the third true leaf expansion stage in shoot apex. The result of Quantitative RT-PCR indicated that GhSPLi might play an important role in bud differentiation, the transition of the growth phase and flower formation.

关键词

陆地棉/GhSPL3/亚细胞定位/荧光定量RT-PCR

Key words

Gossypium hirsutum L./GhSPLi/ subcellular localization/ quantitative RT-PCR

分类

农业科技

引用本文复制引用

李洁,范术丽,宋美珍,庞朝友,喻树迅..陆地棉GhSPL3基因的克隆、亚细胞定位及表达分析[J].棉花学报,2012,24(5):414-419,6.

基金项目

国家高技术研究发展计划(2011AA10A102) (2011AA10A102)

国家棉花产业技术体系(CARS-18) (CARS-18)

棉花学报

OA北大核心CSCDCSTPCD

1002-7807

访问量0
|
下载量0
段落导航相关论文