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丹参中转录因子基因SmMYB-like 1的克隆和表达分析

张顺仓 夏鹏国 王幼平 梁宗锁

扬州大学学报(农业与生命科学版)2017,Vol.38Issue(3):32-38,7.
扬州大学学报(农业与生命科学版)2017,Vol.38Issue(3):32-38,7.DOI:10.16872/j.cnki.1671-4652.2017.03.007

丹参中转录因子基因SmMYB-like 1的克隆和表达分析

Cloning and expression analysis of a transcription factor gene SmMYB-like 1 in Salvia miltiorrhiza

张顺仓 1夏鹏国 2王幼平 1梁宗锁2

作者信息

  • 1. 扬州大学生物科学与技术学院,江苏扬州225009
  • 2. 浙江理工大学生命科学学院,浙江杭州310000
  • 折叠

摘要

Abstract

We obtained a full-length cDNA sequence of R2R3 MYB transcription factors with the homology-based cloning and RACE methods.This gene was named SmMYB-like 1 (GenBank accession No.:JX997333),it contained a 960 bp open reading frame (ORF) encoding 319 amino acids.Sequence analysis predicted that molecular weight of SmMYB-like 1 was 35.84 Ku,and the academic isoelectric point of this protein was 6.24.The multiple sequence alignment and phylogenetic analysis were applied,and the second structure as well as 3-D structure of SmMYB-like 1 was predicted.QRT-PCR was performed to determine expression levels of SmMYB-like 1 in different tissues (root,stem,leaf and flower) of S.miltiorrhiza.Results showed that SmMYB-like 1 expressed in all the tissues tested,with the lowest expression in root and much higher expression in leaf and flower.The recombinant constructs of the SmMYB-like 1-GFP fusion gene was introduced into onion epidermal cells by particle to determine the subcellular localization of SmMYB-like 1 protein,the results showed that it distributed both in nucleus and cytomembrane.

关键词

丹参/R2R3 MYB/基因克隆/亚细胞定位/表达分析

Key words

Salvia miltiorrhiza/R2R3 MYB/gene cloning/subcellular localization/expression analysis

分类

农业科技

引用本文复制引用

张顺仓,夏鹏国,王幼平,梁宗锁..丹参中转录因子基因SmMYB-like 1的克隆和表达分析[J].扬州大学学报(农业与生命科学版),2017,38(3):32-38,7.

基金项目

国家自然科学基金资助项目(31700257、81773835) (31700257、81773835)

江苏省高校自然科学基金面上项目(16KJB180032) (16KJB180032)

中国博士后科学基金面上项目(2015M571826) (2015M571826)

扬州大学学报(农业与生命科学版)

OA北大核心CSTPCD

1671-4652

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