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Precise Genotyping of eIF(iso)4E.a and eIF(iso)4E.c in Main Chinese Cabbage (Brassica rapa ssp. pekinensis) Cultivars and Germplasms |
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Abstract Abstract Virus disease caused by Turnip mosaic virus (TuMV) is one of the most serious problems during Chinese cabbage (Brassica rapa ssp. pekinensis) cultivation. Initial infection of TuMV in Chinese cabbage has been demonstrated to be related to wild type BraA.eIF(iso)4E.a (A) and BraA.eIF(iso)4E.c (C). Loss-of-function mutation in one or two genes hinders TuMV infection and results in virus-resistant phynotype in Chinese cabbage. Two kind of allelic variations, miss splicing mutation (a1) and psedogene mutation (a2) in eIF(iso)4E.a, frame-shift mutation (c1) and transposon-insertion mutation (c2). in eIF(iso)4E.c, has been identified respectively from Chinese cabbage. In this study, the differences among three kinds of eIF(iso)4E.a genotype were compared again. Simple and convenient markers were developed. The precise genotyping of eIF(iso)4E.a and eIF(iso)4E.c was detected among 38 hybrids bought from seed market and 96 germplasms created by our breeding team. The results showed that the allele frequencies for A, a1 and a2 were 36.8%, 40.8%, 22.4% among hybrids and 26.1%, 28.1%, 45.8% among germplasms respectively. Total genotype frequency for two mutant alleles of a1 and a2 was 70.1%. Comparatively, only one germplasm carried c1c1 genotype and 13 germplasms carried c2c2 genotype. The total genotype frequency for c1 and c2 was only 10.4%. The results provide molecular markers for utilizing the genes in germplasms detection and new vriaties breeding. They also provide molecular evidence for continuing expanding of those virus-resistance hybrids.
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Received: 30 June 2017
Published: 02 May 2018
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