2019
DOI: 10.1007/s11032-019-1012-5
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QTL mapping for leaf morphology traits in a large maize-teosinte population

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Cited by 22 publications
(11 citation statements)
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“…This RIL population has also been widely used to fine-map QTL, and identify causal or candidate genes for many traits, including seed shattering (Lin et al 2012), leaf number (Li et al 2016), kernel row number (KRN) (Calderón et al 2016), shoot apical meristem morphology (Leiboff et al 2016), vascular bundle number (Huang et al 2016), tassel-related traits (G. Xu et al 2017), nodal root number (Zhang et al 2018), and leaf morphological traits (Fu et al 2019). Using this population, several QTL have been fine-mapped to single genes including grassy tillers1 ( gt1 ) for controlling prolificacy (PROL) (Wills et al 2013), prolamin box-binding factor1 ( pbf1 ) for kernel weight (Lang et al 2014), glossy15 ( gl15 ) for vegetative phase changes (D.…”
mentioning
confidence: 99%
“…This RIL population has also been widely used to fine-map QTL, and identify causal or candidate genes for many traits, including seed shattering (Lin et al 2012), leaf number (Li et al 2016), kernel row number (KRN) (Calderón et al 2016), shoot apical meristem morphology (Leiboff et al 2016), vascular bundle number (Huang et al 2016), tassel-related traits (G. Xu et al 2017), nodal root number (Zhang et al 2018), and leaf morphological traits (Fu et al 2019). Using this population, several QTL have been fine-mapped to single genes including grassy tillers1 ( gt1 ) for controlling prolificacy (PROL) (Wills et al 2013), prolamin box-binding factor1 ( pbf1 ) for kernel weight (Lang et al 2014), glossy15 ( gl15 ) for vegetative phase changes (D.…”
mentioning
confidence: 99%
“…Among these rice QTL, qFW4-2 was located to a 37-kb region, with the most possible candidate gene which previously detected NAL1 . Moreover, 17 and 14 QTL, respectively, for FLL and FLW have been identified in a maize-teosinte BC 2 S 3 RIL population ( Fu et al, 2019 ). Many mutants with leaf size phenotypes have been characterized, and their relevant genes have been cloned in rice ( Fujino et al, 2008 ; Hu et al, 2010 ; Xiang et al, 2012 ; Liu et al, 2016 ).…”
Section: Introductionmentioning
confidence: 99%
“…In model systems, several genes and networks have been identified to affect initial leaf development and pattern formation [ 2 , 7 , 8 ] as well as leaf length and width [ 9 – 11 ] using the mutagenesis screening method. Moreover, quantitative trait loci have also been detected for leaf morphological traits in species such as tomato [ 12 ], Arabidopsis [ 13 ], Brassica [ 14 ], maize [ 15 ], barley [ 16 ], and Populus [ 17 , 18 ]. Despite advances made in these studies, the identified genes or loci may only cover a portion of the leaf morphological variation observed in nature because the variation is considered to be under polygenic control [ 11 , 19 ].…”
Section: Introductionmentioning
confidence: 99%