生物技术通报 ›› 2016, Vol. 32 ›› Issue (11): 162-169.doi: 10.13560/j.cnki.biotech.bull.1985.2016.11.019

• 研究报告 • 上一篇    下一篇

植物表皮毛发育控制基因GL2遗传互作因子的筛选和鉴定

侍双月, 陈子玉, 安丽君   

  1. 西北农林科技大学生命科学学院 旱区逆境生物学国家重点实验室,杨凌 712100
  • 收稿日期:2016-04-15 出版日期:2016-11-25 发布日期:2016-11-11
  • 作者简介:侍双月,硕士研究生,研究方向:植物分子遗传学;E-mail:zhongyu.best@163.com
  • 基金资助:
    国家自然科学基金项目(31470290),中央高校基本科研业务费(2014YB036,Z109021537)

Screening and Identification of New Genetic Factors Interacting with GL2 During Plant Trichome Development

SHI Shuang-yue, CHEN Zi-yu, AN Li-jun   

  1. State Key Laboratory of Crop Stress Biology for Arid Area /College of Life Sciences,Northwest A&F University,Yangling 712100
  • Received:2016-04-15 Published:2016-11-25 Online:2016-11-11

摘要: 表皮毛广泛存在于陆生植物的地上部分,是植物与环境之间的一道天然屏障,具有多种重要的生物学功能。拟南芥HD-Zip家族转录因子GLABRA 2(GL2)是调控表皮毛形成和发育的关键因子,通过筛选和鉴定GL2的遗传互作因子,可以为进一步研究植物表皮毛发育调控的分子机制奠定基础。通过大规模的遗传筛选和图位克隆,获得了一个叶片上完全没有表皮毛的突变体M12-01,遗传分析表明M12-01 single突变表型受隐性单核基因控制。M12-01 single突变体表型与拟南芥TRANSPARENT TESTA GLABKA 1(TTG1)基因的功能缺失突变体表型相似。对TTG1基因的测序结果显示其+445位碱基由鸟嘌呤突变为腺嘌呤,从而使编码的甘氨酸变为精氨酸。本研究证实TTG1突变能增强gl2-3突变体的表型,GL2基因与TTG1基因之间存在遗传互作,这为进一步研究GL2调控植物表皮毛发育的分子机制提供了新的遗传材料。

关键词: 表皮毛, GL2, 图位克隆, TTG1, 遗传互作

Abstract: Trichomes widely exist on aboveground parts of terrestrial plants,exhibiting as natural barriers between plants and the environment,and also servering many biological functions. The transcription factor GLABRA 2(GL2)is a key factor regulating trichome initiation and the following developmental processes. Screening and identification of new GL2 interactors will lay a foundation for further uncovering the regulatory molecular mechanisms of trichome development. Through large-scale genetic screening and cloning,a new mutant M12-01 without trichome in the leaves was found,and genetic analysis indicated that the phenotype of M12-01single mutant was controlled by a recessive single nuclear gene. The phenotype of M12-01 single mutant was similar to that of functional deletion mutant of Arabidopsis TTG1 gene. Sequencing TTG1 gene revealed that a single nucleotide replacement from guanine to adenine in +445 of TTG1 gene occurred,which resulted in the encoded glycine changed to arginine. This work confirmed that mutation of TTG1 enhanced the phenotype of gl2-3 mutant,and genetic interaction between gene GL2 and TTG1,which provides new genetic materials for further studying the molecular mechanism of GL2 regulation on the development of plant trichome.

Key words: trichome, GL2, map-based cloning, TTG1, genetic interaction