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黄花梨bZIP的cDNA克隆与表达分析

宋燕春 李永裕 黄添毅 陈铁娇 吴少华

热带亚热带植物学报Issue(2):172-178,7.
热带亚热带植物学报Issue(2):172-178,7.DOI:10.3969/j.issn.1005-3395.2014.02.010

黄花梨bZIP的cDNA克隆与表达分析

Cloning and Expresssion Analysis of bZIP Gene from Pyrus pyrifolia‘Huanghua’

宋燕春 1李永裕 2黄添毅 1陈铁娇 1吴少华1

作者信息

  • 1. 福建农林大学园艺学院,福州350002
  • 2. 泸州市农业局,四川泸州646000
  • 折叠

摘要

Abstract

In order to understand the function of PpbZIP of Pyrus pyrifolia‘Huanghua’, PpbZIP gene was cloned from lfower buds of‘Huanghua’ based on homologous gene of bZIP. The results showed that full length of cDNA of PpbZIP (GenBank accession No.:KC951877) was 1843 bp, containing an ORF of 1227 bp and encoding 408 amino acids. PpbZIP also shared 92%homology with bZIP of Malus × domestica. QRT-PCR analysis showed that the expression of PpbZIP gene increased at initiate dormancy stage and then decreased with dormancy releasing. It was suggested that PpbZIP could involve in the regulation of bud dormancy process of‘Huanghua’.

关键词

黄花梨/bZIP/克隆/表达

Key words

Pyrus pyrifolia‘Huanghua’/bZIP/Clone/Expression

引用本文复制引用

宋燕春,李永裕,黄添毅,陈铁娇,吴少华..黄花梨bZIP的cDNA克隆与表达分析[J].热带亚热带植物学报,2014,(2):172-178,7.

基金项目

高等学校博士学科点专项科研基金项目(20113515110011);福建省科技计划重点项目(2012N0005)资助 (20113515110011)

热带亚热带植物学报

OA北大核心CSCDCSTPCD

1005-3395

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