玉米矮秆基因d15的克隆及表达分析
作者:
作者单位:

1.四川农业大学农学院;2.四川正红生物技术有限责任公司

作者简介:

通讯作者:

中图分类号:

基金项目:

四川省重点研发项目(2021YFYZ0017)、重大科技专项(2022ZDX0013);成都市科技创新平台资助项目(2019-YF04-00022-JH)、重点研发项目(2021-YF05-00527-SN)


Cloning and Expression Analysis of Dwarf Gene d15 in Maize
Author:
Affiliation:

Sichuan Zhenghong Bio Co., Ltd

Fund Project:

Key R&D Project of Sichuan Province (2021YFYZ0017), Major Science and Technology Project (2022ZDX0013); Chengdu Science and Technology Innovation Platform Funding Project(2019-YF04-00022-JH), Key R&D Project(2021-YF05-00527-SN)

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    发掘玉米矮秆基因,解析其调控机制,为玉米矮化育种提供种质资源和理论依据。用形态观察和石蜡切片方法,研究玉米矮秆突变体K15d与野生型K15的矮化特征差异;通过等位性鉴定,利用PCR技术克隆矮秆基因d15,解析基因功能,并通过qPCR技术分析3个时期茎节间中d15的表达模式。与野生型K15比较,突变体K15d株高、穗位高和穗下节间数分别降低39.22%、69.75%和38.83%,差异均达显著或极显著水平;茎秆细胞明显变小,排列不规则。矮秆基因d15与br2等位,由5个外显子和4个内含子组成,其中第五外显子5485bp-5685bp区间缺失200bp,编码区全长3983bp,编码1326个氨基酸。编码蛋白的跨膜结构域只有10个,缺失2个,二级结构发生改变,第二个保守功能域缺失,影响了底物的结合和转运功能。d15启动子序列为1091bp,与br2仅有2个SNPs差异,同源性达99.94%。在拔节前、拔节期和拔节后3个时期,突变体中d15基因的表达量与野生型间均无显著差异。由此可见,矮秆基因d15的矮化特征及表达特性均与br2相似,是一个新的br2等位基因,丰富了玉米矮秆基因库。

    Abstract:

    To explore maize dwarf genes and analyze their regulation mechanism, provide germplasm resources and theoretical basis for maize dwarf breeding. Morphological observation and paraffin section were used to study the dwarfing characteristics of maize dwarf mutant K15d and wild type K15. By allele-test, PCR was used to clone the dwarf gene d15, the gene function was analyzed, and the expression pattern of d15 in stem internodes at three stages was analyzed by qPCR. Compared with wild type K15, the plant height, ear height and the internodes number below ear position of mutant K15d decreased by 39.22%, 69.75% and 38.83%, respectively, with significant or extremely significant differences. Stem cells were significantly smaller and irregularly arranged. The dwarf gene d15 was allelic to br2 and consists of 5 exons and 4 introns. The fifth exon was missing 200bp in the range of 5485bp to 5685bp, and the length of coding region was 3983bp which encoded 1326 amino acids. There were only 10 transmembrane domains encoding proteins, two were missing. The change of secondary structure and the loss of the second conserved domain had affected the substrate binding and transport function. The promoter sequence of d15 was 1091bp, and only two SNPs were differences from br2, with 99.94% homology. There was no significant difference between the expression of d15 gene in the mutant and the wild type at the three stages of pre-jointing, jointing and post-jointing. In conclusion, the dwarf gene d15 is a new br2 allele with similar dwarfing characteristics and expression characteristics to br2, which enriches the maize dwarf gene pool.

    参考文献
    相似文献
    引证文献
引用本文
分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2022-11-15
  • 最后修改日期:2023-01-11
  • 录用日期:2023-02-06
  • 在线发布日期: 2023-02-17
  • 出版日期:
您是第位访问者
ICP:京ICP备09069690号-23
京ICP备09069690号-23
植物遗传资源学报 ® 2024 版权所有
技术支持:北京勤云科技发展有限公司