Literature DB >> 30862676

Proteomic analysis reveals that sugar and fatty acid metabolisms play a central role in sterility of the male-sterile line 1355A of cotton.

Yuanlong Wu1, Yanlong Li1, Yaoyao Li1, Yizan Ma1, Yunlong Zhao1, Chaozhi Wang1, Huabin Chi1, Miao Chen1, Yuanhao Ding1, Xiaoping Guo2, Ling Min3, XianLong Zhang1.   

Abstract

Cotton (Gossypium spp.) is one of the most important economic crops and exhibits yield-improving heterosis in specific hybrid combinations. The genic male-sterility system is the main strategy used for producing heterosis in cotton. To better understand the mechanisms of male sterility in cotton, we carried out two-dimensional electrophoresis (2-DE) and label-free quantitative proteomics analysis in the anthers of two near-isogenic lines, the male-sterile line 1355A and the male-fertile line 1355B. We identified 39 and 124 proteins that were significantly differentially expressed between these two lines in the anthers at the tetrad stage (stage 7) and uninucleate pollen stage (stage 8), respectively. Gene ontology-based analysis revealed that these differentially expressed proteins were mainly associated with pyruvate, carbohydrate, and fatty acid metabolism. Biochemical analysis revealed that in the anthers of line 1355A, glycolysis was activated, which was caused by a reduction in fructose, glucose, and other soluble sugars, and that accumulation of acetyl-CoA was increased along with a significant increase in C14:0 and C18:1 free fatty acids. However, the activities of pyruvate dehydrogenase and fatty acid biosynthesis were inhibited and fatty acid β-oxidation was activated at the translational level in 1355A. We speculate that in the 1355A anther, high rates of glucose metabolism may promote fatty acid synthesis to enable anther growth. These results provide new insights into the molecular mechanism of genic male sterility in upland cotton.
© 2019 Wu et al.

Entities:  

Keywords:  Gossypium; artificial emasculation; carbohydrate metabolism; fatty acid metabolism; glycolysis; heterosis; male sterility; protein expression; proteomics; pyruvate

Mesh:

Substances:

Year:  2019        PMID: 30862676      PMCID: PMC6497933          DOI: 10.1074/jbc.RA118.006878

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


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