2014
DOI: 10.1007/s11032-014-0150-z
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Breeding value estimation of the application of IPA1 and DEP1 to improvement of Oryza sativa L. ssp. japonica in early hybrid generations

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Cited by 19 publications
(14 citation statements)
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“…The Di value reflected the variation caused by random genetic backgrounds rather than the regulatory genes, its influences on MRW, C and HR need to be deeply discussed. Many studies had proved that gene contribution rates differ depending on their genetic backgrounds (Huang et al 2009;Xu et al 2014), and the genetic backgrounds' random introduction from indica may also contain the other QTLs that not be successfully cloned (Ren et al 2016). We speculated that the variations containing genetic backgrounds and multiple QTLs all contributed to its influences on MRW, C and HR.…”
Section: Discussionmentioning
confidence: 98%
See 1 more Smart Citation
“…The Di value reflected the variation caused by random genetic backgrounds rather than the regulatory genes, its influences on MRW, C and HR need to be deeply discussed. Many studies had proved that gene contribution rates differ depending on their genetic backgrounds (Huang et al 2009;Xu et al 2014), and the genetic backgrounds' random introduction from indica may also contain the other QTLs that not be successfully cloned (Ren et al 2016). We speculated that the variations containing genetic backgrounds and multiple QTLs all contributed to its influences on MRW, C and HR.…”
Section: Discussionmentioning
confidence: 98%
“…The majority of loci affecting rice quality are QTLs, and the differences in their explained phenotypic variation were relatively great under different genetic backgrounds (Cui et al 2003;Huang et al 2009;Xu et al 2014). Additionally, the number of confirmed regulatory genes is extremely limited.…”
Section: Introductionmentioning
confidence: 99%
“…Yan et al ( 2009 ) developed the Gn1a-M1 marker for the detection of Gn1a -Habataki allele, which has a 16-bp deletion in the 5’-untranslated region (5’UTR), and the Gn1a-M2 marker for the detection of Gn1a -5150 allele, which has an 11-bp deletion on the third exon. Xu et al ( 2014 ) developed the CAPS marker using Sdu I restriction enzyme to select OsSPL14 -Ri22 allele, which transcribes OsmiR156-resistant OsSPL14 transcripts caused by the nucleotide substitution at the OsmiR156 target site. They also developed the gene-tagged PCR marker of DEP1 gene using the 625-bp gap on the fifth exon between the yield-positive allele and non-target allele.…”
Section: Introductionmentioning
confidence: 99%
“…For the Gn1a gene, a 16-bp deletion in 5’UTR is common in indica rice varieties (54.3%) (Yan et al 2009 ), suggesting that the Gn1a -M1 marker may not function in many indica varieties. For the DEP1 marker (Xu et al 2014 ), the intensity of the non-target allele band was very weak compared with that of the target allele in the heterozygous plants. To obtain clear genotype data, the previous DEP1 marker needs to be improved.…”
Section: Introductionmentioning
confidence: 99%
“…The indica allele frequency was calculated as the ratio of the number of indicatype markers to the total number of markers. The DEP1 locus was genotyped as described previously (Xu et al 2014). …”
Section: Dna Extraction and Subspecies-specific Genotypingmentioning
confidence: 99%