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1.
BMC Plant Biol ; 11: 49, 2011 Mar 16.
Article in English | MEDLINE | ID: mdl-21410961

ABSTRACT

BACKGROUND: Semigamy in cotton is a type of facultative apomixis controlled by an incompletely dominant autosomal gene (Se). During semigamy, the sperm and egg cells undergo cellular fusion, but the sperm and egg nucleus fail to fuse in the embryo sac, giving rise to diploid, haploid, or chimeric embryos composed of sectors of paternal and maternal origin. In this study we sought to identify differentially expressed genes related to the semigamy genotype by implementing a comparative microarray analysis of anthers and ovules between a non-semigametic Pima S-1 cotton and its doubled haploid natural isogenic mutant semigametic 57-4. Selected differentially expressed genes identified by the microarray results were then confirmed using quantitative reverse transcription PCR (qRT-PCR). RESULTS: The comparative analysis between isogenic 57-4 and Pima S-1 identified 284 genes in anthers and 1,864 genes in ovules as being differentially expressed in the semigametic genotype 57-4. Based on gene functions, 127 differentially expressed genes were common to both semigametic anthers and ovules, with 115 being consistently differentially expressed in both tissues. Nine of those genes were selected for qRT-PCR analysis, seven of which were confirmed. Furthermore, several well characterized metabolic pathways including glycolysis/gluconeogenesis, carbon fixation in photosynthetic organisms, sesquiterpenoid biosynthesis, and the biosynthesis of and response to plant hormones were shown to be affected by differentially expressed genes in the semigametic tissues. CONCLUSION: As the first report using microarray analysis, several important metabolic pathways affected by differentially expressed genes in the semigametic cotton genotype have been identified and described in detail. While these genes are unlikely to be the semigamy gene itself, the effects associated with expression changes in those genes do mimic phenotypic traits observed in semigametic plants. A more in-depth analysis of semigamy is necessary to understand its expression and regulation at the genetic and molecular level.


Subject(s)
Gene Expression Profiling , Gossypium/genetics , Oligonucleotide Array Sequence Analysis , Flowers/genetics , Gene Expression Regulation, Developmental , Gene Expression Regulation, Plant , Ovule/genetics , RNA, Plant/genetics , Reverse Transcriptase Polymerase Chain Reaction
2.
Plant Cell Rep ; 27(3): 553-61, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18080126

ABSTRACT

CMS-D8 and its restorer were developed by introducing the cytoplasm and nuclear gene Rf (2) from the wild diploid Gossypium trilobum (D8) into the cultivated tetraploid Upland cotton (Gossypium hirsutum). No information is available on how the Rf (2) gene interacts with CMS-associated genes and how CMS-D8 cytoplasm affects nuclear gene expression. The objective of this study was to identify differentially expressed genes in anther tissues between the non-restoring fertile maintainer ARK8518 (rf(2) rf(2)) and its isogenic heterozygous D8 restorer line, ARK8518R (Rf(2) rf(2)) with D8 cytoplasm, by mRNA differential display (DD). Out of more than 3,000 DDRT-PCR bands amplified by 31 primer combinations from 12 anchor primers and 8 arbitrary decamer primers, approximately 100 bands were identified as being qualitatively differentially displayed. A total of 38 cDNA fragments including 12 preferentially expressed cDNA bands in anther were isolated, cloned and sequenced. Reverse northern blot analysis showed that only 4 genes, including genes encoding a Cys-3-His zinc finger protein and aminopeptidase, were up-regulated, while 22 genes, including genes for phosphoribosylanthranilate transferase (PAT), starch synthase (SS), 4-coumarate-CoA ligase, electron transporter, calnexin, arginine decarboxylase, and polyubiquitin, were down-regulated in the heterozygous restorer ARK8518R. The down-regulation of SS explains the lack of starch accumulation in sterile rf(2) pollen grains in the heterozygous restored plants. The molecular mechanism of CMS and its restoration, specifically the possible roles of SS and PAT genes in relation to restoration of Rf(2) to CMS-D8, are discussed. This investigation represents the first account of such an analysis in cotton.


Subject(s)
Gene Expression Profiling/methods , Gossypium/genetics , Blotting, Northern , DNA, Complementary/chemistry , DNA, Complementary/genetics , Fertility/genetics , Gene Expression Regulation, Plant , Genes, Plant , Plants, Genetically Modified , Reverse Transcriptase Polymerase Chain Reaction , Sequence Analysis, DNA
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