详细信息
Isolation, characterization and expression analysis of the BABY BOOM (BBM) gene from Larix kaempferi x L. olgensis during adventitious rooting ( SCI-EXPANDED收录) 被引量:16
文献类型:期刊文献
英文题名:Isolation, characterization and expression analysis of the BABY BOOM (BBM) gene from Larix kaempferi x L. olgensis during adventitious rooting
作者:Li, Kui-peng[1,2] Sun, Xiao-mei[1,2] Han, Hua[1] Zhang, Shou-gong[1,2]
第一作者:Li, Kui-peng
通信作者:Zhang, SG[1]
机构:[1]Chinese Acad Forestry, State Key Lab Tree Genet & Breeding, Beijing 100091, Peoples R China;[2]Chinese Acad Forestry, Res Inst Forestry, Beijing 100091, Peoples R China
年份:2014
卷号:551
期号:2
起止页码:111-118
外文期刊名:GENE
收录:;WOS:【SCI-EXPANDED(收录号:WOS:000343624800001)】;
基金:This study was undertaken as a project for the National Science & Technology Pillar Program in the Twelfth Five-Year Plan Period of China (2012BAD01B01) and was supported by the National High Technology Research and Development Program of China (2011AA100203).
语种:英文
外文关键词:Larix kaempferi x L. olgensis; BABY BOOM; Motif analysis; Adventitious rooting; Expression pattern
摘要:The full-length cDNA and genomic sequences of the BABY BOOM (BBM) gene, designated LkBBM, were isolated from Larix kaempferi x Larix olgensis. The 3324 bp cDNA was cloned and its open reading frame (ORF) consists of 2370 nucleotides. The deduced 789 amino acid protein contains two AP2 domains and a BBM specific motif. Four conserved motifs between BBM and PLT were identified, which may be conducive to the similar function of BBM and PLT. The three dimensional (3D) structure of LkBBM was predicted and beta-sheets in the AP2-R2 domain of LkBBM might recognize the specific base pairs in the major groove. Analysis of the LkBBM gene structure indicates that the gene has eight introns and nine exons. In the 5'-flanking promoter region of LkBBM, many important potential cis-acting elements were identified, such as the TATABOX5 element (a functional TATA element), ROOTMOTIFTAPOX1 element (element of root specificity), AUXREPSIAA4 element (element involved in auxin responsiveness and gene expression in root meristem), MYB1AT element (element involved in MYB recognition), ARR1AT element (element involved in cytokinin responsiveness), GARE1OSREP1 element (element involved in gibberellin responsiveness) and PYRIMIDINEBOXHVEPB1 element (element involved in abscisic acid responsiveness), which all suggested that the expression of LkBBM is highly regulated. Compared with gene expression levels in the stem, stem tip and leaf, LkBBM shows a specific expression in the root, which indicates that LkBBM plays a key rote in regulating the development and growth of root in larch. In the processing of larch adventitious root formation, LkBBM started to express on the eighth day after rooting treatment and its transcript level increased continuously afterwards. According to the gene characteristics, LkBBM is proposed as a molecular marker for root primordia of larch, and the initial period of LkBBM expression may be the formation period of root primordia in the processing of adventitious rooting of larch. (C) 2014 Elsevier B.V. All rights reserved.
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