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来自蕙兰(Cymbidium faberi)的一个APETALA1/FRUITFULL类MADS-box基因的分子克隆及时空表达

Molecular cloning and spatiotemporal expression of an APETALA1/FRUITFULL-like MADS-box gene from the orchid (Cymbidium faberi).

作者信息

Tian Yunfang, Yuan Xiuyun, Jiang Suhua, Cui Bo, Su Jinle

机构信息

College of Forestry, Henan Agricultural University, Zhengzhou 450002, Henan, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2013 Feb;29(2):203-13.

Abstract

In order to identify genes involved in floral transition and development of the orchid species, a full-length APETALA1/FRUITFULL-like (AP1/FUL-like) MADS box cDNA was cloned from Cymbidium faberi (C. faberi) sepals and designated as C. faberi APETALA1-like (CfAP11], JQ031272.1). The deduced amino acid sequence of CfAP11 shared 84% homology with a member of the AP1/FUL-like group of MADS box genes (AY927238.1, Dendrobium thyrsiflorum FUL-like MADS box protein 3 mRNA). Phylogenetic analysis shows that CfAP11 belonged to the AP1/FUL transcription factor subfamily. Bioinformatics analysis shows that the deduced protein had a MADS domain and a relatively conservative K region. The secondary structure of CfAP11 mainly consisted of alpha helices (58.97%), and the three-dimensional structure of the protein was similar to that of homologues in Roza hybrida, Oryza sativa and Narcissus tazetta. Real-time quantitative PCR (qRT-PCR) results reveal low levels of its mRNA in roots, lower levels in leaves during reproductive period than vegetative period, and higher levels in pedicels at full-blossom stage than at bud stage. These results suggest that CfAP11 is involved in floral induction and floral development. Additionally, we observed higher levels of CfAP11 expression in pedicels and ovaries than in other tissues during full-blossom stage, which suggests that CfAP11 may also be involved in fruit formation in certain mechanism.

摘要

为了鉴定参与兰花物种花期转变和发育的基因,从蕙兰萼片中克隆了一个全长APETALA1/FRUITFULL类(AP1/FUL类)MADS盒cDNA,并将其命名为蕙兰APETALA1类(CfAP11,JQ031272.1)。CfAP11推导的氨基酸序列与MADS盒基因AP1/FUL类群的一个成员(AY927238.1,密花石斛FUL类MADS盒蛋白3 mRNA)具有84%的同源性。系统发育分析表明,CfAP11属于AP1/FUL转录因子亚家族。生物信息学分析表明,推导的蛋白具有一个MADS结构域和一个相对保守的K区域。CfAP11的二级结构主要由α螺旋组成(58.97%),其三维结构与杂种月季、水稻和水仙中的同源物相似。实时定量PCR(qRT-PCR)结果显示,其mRNA在根中的水平较低,在生殖期叶片中的水平低于营养期,在盛花期花梗中的水平高于花蕾期。这些结果表明,CfAP11参与了花的诱导和花的发育。此外,我们观察到在盛花期,花梗和子房中的CfAP11表达水平高于其他组织,这表明CfAP11可能也通过某种机制参与果实形成。

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