Cloning of a phosphatidylinositol 4-kinase gene based on fiber strength transcriptome QTL mapping in the cotton species Gossypium barbadense

被引:3
|
作者
Liu, H. W. [1 ,2 ]
Shi, R. F. [1 ]
Wang, X. F. [1 ]
Pan, Y. X. [1 ]
Zhang, G. Y. [1 ]
Ma, Z. Y. [1 ]
机构
[1] Agr Univ Hebei, N China Key Lab Crop Germplasm Resources, Educ Minist, Baoding, Peoples R China
[2] Suzhou Univ Sci & Technol, Sch Chem & Biol Engn, Suzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
cDNA cloning; Fiber strength; Gossypium barbadense; Phosphatidylinositol; 4-kinase; Real-time PCR; ARABIDOPSIS;
D O I
10.4238/2012.July.13.1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sea Island cotton (Gossypium barbadense) is highly valued for its superior fiber qualities, especially fiber strength. Based on a transcript-derived fragment originated from transcriptome QTL mapping, a fiber strength related candidate gene of phosphatidylinositol 4-kinase cDNA, designated as GbPI4K, was first cloned, and its expression was characterized in the secondary cell wall thickening stage of G. barbadense fibers. The ORF of GbPI4K was found to be 1926 bp in length and encoded a predicted protein of 641 amino acid residues. The putative protein contained a clear PI3/4K kinase catalytic domain and fell into the plant type II PI4K cluster in phylogenetic analysis. In this study, the expression of cotton PI4K protein was also induced in Escherichia coli BL21 (DE3) as a fused protein. Semi-quantitative RT-PCR analysis showed that the gene expressed in the root, hypocotyl and leaf of the cotton plants. Real-time RT-PCR indicated that this gene in Sea Island cotton fibers expressed 10 days longer than that in Upland cotton fibers, and the main expression difference of PI4K between Sea Island cotton and Upland cotton in fibers was located in the secondary cell wall thickening stage of the fiber. Further analysis indicated that PI4K is a crucial factor in the ability of Rac proteins to regulate phospholipid signaling pathways.
引用
收藏
页码:3367 / 3378
页数:12
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