2016
DOI: 10.1186/s12870-016-0864-7
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Comparative transcript profiling of alloplasmic male-sterile lines revealed altered gene expression related to pollen development in rice (Oryza sativa L.)

Abstract: BackgroundCytoplasmic male sterility (CMS) is an ideal model for investigating the mitochondrial-nuclear interaction and down-regulated genes in CMS lines which might be the candidate genes for pollen development in rice. In this study, a set of rice alloplasmic sporophytic CMS lines was obtained by successive backcrossing of Meixiang B, with three different cytoplasmic types: D62A (D type), ZS97A (WA type) and XQZ-A (DA type).ResultsUsing microarray, the anther transcript profiles of the three indica rice CMS… Show more

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Cited by 19 publications
(13 citation statements)
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“…[37]. Analysis of the pollen transcriptome of three male sterile lines using weighted gene co-expression network analysis revealed that two modules were significantly associated with male sterility and many hub genes that were differentially expressed in the sterile lines [38]. Farcuh et al used WGCNA to investigate sugar metabolism during leaf and fruit development of two Japanese plum varieties, and identified 11 key sugar metabolism-related genes, the results showed that sugar metabolism was reprogrammed in a non-climacteric bud mutant of a climacteric plum fruit and showed an increase in sorbitol synthesis [39].…”
Section: Discussionmentioning
confidence: 99%
“…[37]. Analysis of the pollen transcriptome of three male sterile lines using weighted gene co-expression network analysis revealed that two modules were significantly associated with male sterility and many hub genes that were differentially expressed in the sterile lines [38]. Farcuh et al used WGCNA to investigate sugar metabolism during leaf and fruit development of two Japanese plum varieties, and identified 11 key sugar metabolism-related genes, the results showed that sugar metabolism was reprogrammed in a non-climacteric bud mutant of a climacteric plum fruit and showed an increase in sorbitol synthesis [39].…”
Section: Discussionmentioning
confidence: 99%
“…Samples were analyzed with a fluorescence confocal scanner microscope (Nikon, Tokyo, Japan) using a 450/515 nm excitation/emission spectrum for TUNEL fluorescein and a 358/461 nm excitation/emission spectrum for DAPI as described in [ 15 ]. For DNA laddering analysis, total DNA was isolated from the anthers in different developmental stages [ 50 ]. Then, the total DNA was redissolved in Tris-EDTA (10 mmol L −1 Tris-HCl (pH 8.0), 5 mmol L −1 EDTA) and incubated at 37 °C for 60 min in the presence of RNase A (100 g mL −1 ).…”
Section: Methodsmentioning
confidence: 99%
“…Total DNA was isolated from the anthers in different developmental stages using the cetyl trimethylammonium bromide extraction procedure ( Hu et al, 2016 ). Next, the total DNA was redissolved in Tris-EDTA buffer solution (10 mmol L -1 Tris-HCl (pH 8.0), 5 mmol L -1 EDTA) and incubated at 37°C for 60 min in the presence of RNase A (100 g mL -1 ).…”
Section: Methodsmentioning
confidence: 99%