A maize bundle sheath defective mutation mapped on chromosome 1 between SSR markers umc1395 and umc1603
文献类型: 外文期刊
作者: Pan Yu 1 ; Chen Xu-qing 1 ; Xie Hua 1 ; Deng Lei 3 ; Li Xiang-long 1 ; Zhang Xiao-dong 1 ; Han Li-xin 1 ; Yang Feng-ping; 1 ;
作者机构: 1.Beijing Acad Agr & Forestry Sci, Beijing Agrobiotechnol Res Ctr, Beijing 100097, Peoples R China
2.Southwest Univ, Minist Educ, Key Lab Hort Sci Southern Mt Reg, Coll Hort & Landscape Architecture, Chongqing 400715, Peoples R China
3.Chongqin
关键词: maize;bsd-pg;SLAF;SSR assossiation analysis;fine mapping
期刊名称:JOURNAL OF INTEGRATIVE AGRICULTURE ( 影响因子:2.848; 五年影响因子:2.979 )
ISSN: 2095-3119
年卷期: 2015 年 14 卷 10 期
页码:
收录情况: SCI
摘要: The bsd-pg (bundle sheath defective pale green) mutant is a novel maize mutation, controlled by a single recessive gene, which was isolated from offspring of maize plantlets regenerated from tissue callus of the maize inbred line 501. The characterization was that the biogenesis and development of the chloroplasts was mainly interfered in bundle sheath cells rather than in mesophyll cells. For mapping the bsd-pg, an F-2 population was derived from a cross between the mutant bsd-pg and an inbred line Xianzao 17. Using specific locus amplified fragment sequencing (SLAF-Seq) technology, a total of 5 783 polymorphic SLAFs were analysed with 1 771 homozygous alleles between maternal and paternal parents. There were 49 SLAFs, which had a ratio of paternal to maternal alleles of 2:1 in bulked normal lines, and three trait-related candidate regions were obtained on chromosome 1 with a size of 3.945 Mb. For the fine mapping, new simple sequence repeats (SSRs) markers were designed by utilizing information of the B73 genome and the candidate regions were localized a size of 850 934 bp on chromosome 1 between umc1603 and umc1395, including 35 candidate genes. These results provide a foundation for the cloning of bsd-pg by map-based strategy, which is essential for revealing the functional differentiation and coordination of the two cell types, and helps to elucidate a comprehensive understanding of the C4 photosynthesis pathway and related processes in maize leaves.
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