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A CIN-like TCP transcription factor(LsTCP4)having retrotransposon insertion associates with a shift from Salinas type to Empire type in crisphead lettuce(Lactuca sativa L.) 被引量:10

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摘要 To improve several agronomic traits in crisphead lettuce(Lactuca sativa L.)under high-temperature growth conditions,we investigated the correlation among those traits in multiple cultivars and performed genetic mapping of their causal genes.In a field cultivation test of Empire type(serrated leaf)and Salinas type(wavy leaf)cultivars,Empire type cultivars showed increased tipburn susceptibility and late bolting compared with Salinas type cultivars.We attempted genetic mapping of leaf shape and bolting time by ddRAD-seq using the F2 population derived from a cross between‘VI185’(Empire type)and‘ShinanoGreen’(Salinas type).These analyses suggested that both traits are controlled by a single locus in LG5.Genotyping of 51 commercial lettuce cultivars with a tightly linked marker(LG5_v8_252.743Mbp)at this locus showed an association between its genotype and the serrated leaf phenotype.By further fine mapping and transcriptome analysis,a gene encoding putative CIN-like TCP transcription factor was determined to be a candidate gene at this locus and was designated as LsTCP4.An insertion of retrotransposable element was found in the allele of‘VI185’,and its transcript level in the leaves was lower than that in‘ShinanoGreen’.Because shapes of leaf epidermal cells in‘VI185’were similar to those in the TCP family mutant of Arabidopsis thaliana,the leaf shape phenotype was likely caused by reduced expression of LsTCP4.Furthermore,because it is known that the TCP family protein also controls flowering time via interaction with FT in A.thaliana,it was highly possible that LsTCP4 gave pleiotropic effects on both leaf shape and bolting time in lettuce.
出处 《Horticulture Research》 SCIE 2020年第1期2597-2610,共14页 园艺研究(英文)
基金 supported by grants from the Ministry of Agriculture,Forestry and Fisheries of Japan(Project for Climate Change,Vegetable-4103)for K.S.,Cooperative Research Grant of the Genome Research for BioResource,NODAI Genome Research Center,Tokyo University of Agriculture for K.S.and K.K.,Grant-in-Aid for Scientific Research for K.K.,MEXT-Supported Program for the Strategic Research Foundation at Private Universities,2013-2017(S1311017)for K.K.We thank Rumi Ohtake of NODAI Genome Research Center,Tokyo University of Agriculture,and Masaki Kawakami of the Nagano Vegetable Ornamental Crops Experiment Station for helpful discussion and advice.We also thank Chizuru Kagami,Yoko Takahashi,Yoshie Nakayama,and especially Atsushi Tsukada and Hideaki Okazawa for technical assistance in the field experiment.We also thank Akane Igarashi,Reina Ohwaki,and Hiroto Kayama for technical assistance in the RNA-seq analysis and genome sequencing,Naho Takahashi for technical assistance in the extraction of genomic DNA.Moreover,we also thank‘Bas Breau’at hakuba for helpful assistance.
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