Rice Genomics, Genetics and Breeding 2018
DOI: 10.1007/978-981-10-7461-5_12
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Domestication Loci Controlling Panicle Shape, Seed Shattering, and Seed Awning

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Cited by 6 publications
(6 citation statements)
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“…Because sh4 and qSH1 were identified in QTL analyses as having large effects on seed shattering, they were believed to be the genes explaining the loss of seed shattering during rice domestication. However, recent research through longer term experiments using plant materials with wild rice introgression lines have proved this view to be over-simplified (Ishii and Ishikawa 2018; see discussion below).…”
Section: Loss Of Seed Shatteringmentioning
confidence: 99%
See 1 more Smart Citation
“…Because sh4 and qSH1 were identified in QTL analyses as having large effects on seed shattering, they were believed to be the genes explaining the loss of seed shattering during rice domestication. However, recent research through longer term experiments using plant materials with wild rice introgression lines have proved this view to be over-simplified (Ishii and Ishikawa 2018; see discussion below).…”
Section: Loss Of Seed Shatteringmentioning
confidence: 99%
“…Therefore, it would be more accurate to evaluate domestication-related mutated alleles in the wild rice genetic background. Therefore, research carried out at Kobe University has focused on maintaining a wild population of rice (the annual form of O. rufipogon sensu lato) and introgressing alleles from domesticated lines into this population to assess the impact of hypothesised domestication alleles on rice characters and through hand-harvesting experiments (Ishii and Ishikawa 2018). This is the opposite of most functional genetics which introgresses targeted wild rice alleles into plants of domesticated rice background, which means that interactions with other genes selected in domesticated populations can go undetected.…”
Section: What Traits Were Targeted For Selection In Early Rice Domestication?mentioning
confidence: 99%
“…Magwa et al 2016: 641, table 1) for a comparison between two Chinese regions, Hainan and Wuhan). iv) Within the same wild as well as domesticated species, the awn length is variable between primary and secondary branches or tillers, and among the five uppermost spikelets on the top primary branch in the panicles (Ikemoto et al 2017;Ishii and Ishikawa 2018).…”
Section: Phenotypic Diversitymentioning
confidence: 99%
“…This implies that single change in the wild ancestor may not have had immediate phenotypic effects until the overall genetic framework was sufficiently modified by other mutations (Ray and Chakraborty 2018). Under this scenario, other mechanisms to enhance seed retention would also have been selected upon, such as a mechanism based on changes of the architecture of the inflorescence (Ishii et al 2013;Ishii and Ishikawa 2018); such as in Oryza rufipogon, the wild progenitor of domesticated rice (O. sativa), the panicle could be either open or spreading. However, Ishii et al (2013) discovered that one of the many early genetic mutations in rice, namely a mutation in a single locus, the SPR3 locus on chromosome 4, converts the open-panicle architecture of the wild species to the closed panicle of domesticated rice, leading to approximately 50% gain in number of seeds recovered at maturity over a typical wild spreading inflorescence type.…”
Section: The Persistence Of Long Awns Beyond the Domestication Periodmentioning
confidence: 99%
“…This may enhance self-pollination and the accumulation of recessive alleles at the seed-shattering loci. After the emergence of non-seed-shattering plants, seed awning may have become an undesirable trait because long awns disturb seed harvesting and handling (Ishii and Ishikawa 2018).…”
Section: Introductionmentioning
confidence: 99%