2020
DOI: 10.21203/rs.3.rs-21523/v2
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Substitution mapping of the major quantitative trait loci controlling stigma exsertion rate from Oryza glumaepatula

Abstract: Background: Stigma exsertion rate (SER) is a key determinant for the outcrossing ability of male sterility lines (MSLs) in hybrid rice seed production. In the process of domestication, the outcrossing ability of cultivated rice varieties decreased, while that of wild Oryza species kept strong. Here, we detected the quantitative trait loci (QTLs) controlling SER using a set of single-segment substitution lines (SSSLs) derived from O. glumaepatula , a wild Oryza species. Results: Seven QTLs for SER were located … Show more

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Cited by 4 publications
(10 citation statements)
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“…It was difficult to determine the precise location of QTLs in rice genome by using the F2 plants, Recombinant Inbred Lines (RILs), Backcross Inbred Lines (BILs) and Doubled Haploid Lines (DHLs) (Ashikari et al 2006). Consequently, the development of Nearly Isogenic Lines (NILs), Chromosome Fragment Substitution Line (CSSL) and Single Segment Substitution Line (SSSL) were necessary for QTL fine mapping and gene cloning (Ashikari et al 2006;Guo et al 2016;Zhou et al2017;Wang et al 2018;Yang et al 2018;Luan et al 2019;Tan et al 2020;Tan et al 2021), especially for the minor genes.…”
Section: Discussionmentioning
confidence: 99%
“…It was difficult to determine the precise location of QTLs in rice genome by using the F2 plants, Recombinant Inbred Lines (RILs), Backcross Inbred Lines (BILs) and Doubled Haploid Lines (DHLs) (Ashikari et al 2006). Consequently, the development of Nearly Isogenic Lines (NILs), Chromosome Fragment Substitution Line (CSSL) and Single Segment Substitution Line (SSSL) were necessary for QTL fine mapping and gene cloning (Ashikari et al 2006;Guo et al 2016;Zhou et al2017;Wang et al 2018;Yang et al 2018;Luan et al 2019;Tan et al 2020;Tan et al 2021), especially for the minor genes.…”
Section: Discussionmentioning
confidence: 99%
“…The DNA samples were amplified by PCR method. The PCR products were separated by gel electrophoresis on 6% denatured PAGE and detected by the silver staining method (Tan et al 2020). To develop secondary SSSLs or NILs, 03-08 and 15-08 were crossed with the recipient HJX74.…”
Section: Genotyping Of Molecular Markers and Substitution Mappingmentioning
confidence: 99%
“…Minimum length, maximum length and estimated length of a substitution segment were estimated as described by Tan (2020). When PGC showed significant difference between SSSL genotype and HJX74 genotype, a QTL for PGC was detected on the substitution segment of SSSL.…”
Section: Genotyping Of Molecular Markers and Substitution Mappingmentioning
confidence: 99%
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