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Candidate genes for first flower node identified in pepper using combined SLAF-seq and BSA

First flower node (FFN) is an important trait for evaluating fruit earliness in pepper (Capsicum annuum L.), but the genetic mechanisms that control FFN are still poorly understood. In the present study, we developed 249 F(2) plants derived from an intraspecific cross between the inbred pepper lines...

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Autores principales: Zhang, Xiaofen, Wang, Guoyun, Chen, Bin, Du, Heshan, Zhang, Fenglan, Zhang, Haiying, Wang, Qian, Geng, Sansheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5860747/
https://www.ncbi.nlm.nih.gov/pubmed/29558466
http://dx.doi.org/10.1371/journal.pone.0194071
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author Zhang, Xiaofen
Wang, Guoyun
Chen, Bin
Du, Heshan
Zhang, Fenglan
Zhang, Haiying
Wang, Qian
Geng, Sansheng
author_facet Zhang, Xiaofen
Wang, Guoyun
Chen, Bin
Du, Heshan
Zhang, Fenglan
Zhang, Haiying
Wang, Qian
Geng, Sansheng
author_sort Zhang, Xiaofen
collection PubMed
description First flower node (FFN) is an important trait for evaluating fruit earliness in pepper (Capsicum annuum L.), but the genetic mechanisms that control FFN are still poorly understood. In the present study, we developed 249 F(2) plants derived from an intraspecific cross between the inbred pepper lines Z4 and Z5. Thirty plants with the highest FFN and 30 plants with the lowest FFN were chosen and their DNAs were pooled according to phenotype to construct two bulked DNA pools. Specific-locus amplified fragment sequencing (SLAF-seq) was combined with bulked segregant analysis (BSA) to identify candidate regions related to FFN. According to our genetic analysis, the FFN trait is quantitatively inherited. A total of 106,848 high-quality single nucleotide polymorphism (SNP) markers were obtained, and 393 high-quality SNP markers associated with FFN were detected. Ten candidate regions within an interval of 3.98 Mb on chromosome 12 harboring 23 candidate genes were identified as closely correlated with FFN. Five genes (CA12g15130, CA12g15160, CA12g15370, CA12g15360, and CA12g15390) are predicted based on their annotations to be associated with expression of the FFN trait. The present study demonstrates an efficient genetic mapping strategy and lays a good foundation for molecular marker-assisted breeding using SNP markers linked to FFN and for cloning and functional analysis of the key genes controlling FFN.
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spelling pubmed-58607472018-03-28 Candidate genes for first flower node identified in pepper using combined SLAF-seq and BSA Zhang, Xiaofen Wang, Guoyun Chen, Bin Du, Heshan Zhang, Fenglan Zhang, Haiying Wang, Qian Geng, Sansheng PLoS One Research Article First flower node (FFN) is an important trait for evaluating fruit earliness in pepper (Capsicum annuum L.), but the genetic mechanisms that control FFN are still poorly understood. In the present study, we developed 249 F(2) plants derived from an intraspecific cross between the inbred pepper lines Z4 and Z5. Thirty plants with the highest FFN and 30 plants with the lowest FFN were chosen and their DNAs were pooled according to phenotype to construct two bulked DNA pools. Specific-locus amplified fragment sequencing (SLAF-seq) was combined with bulked segregant analysis (BSA) to identify candidate regions related to FFN. According to our genetic analysis, the FFN trait is quantitatively inherited. A total of 106,848 high-quality single nucleotide polymorphism (SNP) markers were obtained, and 393 high-quality SNP markers associated with FFN were detected. Ten candidate regions within an interval of 3.98 Mb on chromosome 12 harboring 23 candidate genes were identified as closely correlated with FFN. Five genes (CA12g15130, CA12g15160, CA12g15370, CA12g15360, and CA12g15390) are predicted based on their annotations to be associated with expression of the FFN trait. The present study demonstrates an efficient genetic mapping strategy and lays a good foundation for molecular marker-assisted breeding using SNP markers linked to FFN and for cloning and functional analysis of the key genes controlling FFN. Public Library of Science 2018-03-20 /pmc/articles/PMC5860747/ /pubmed/29558466 http://dx.doi.org/10.1371/journal.pone.0194071 Text en © 2018 Zhang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Zhang, Xiaofen
Wang, Guoyun
Chen, Bin
Du, Heshan
Zhang, Fenglan
Zhang, Haiying
Wang, Qian
Geng, Sansheng
Candidate genes for first flower node identified in pepper using combined SLAF-seq and BSA
title Candidate genes for first flower node identified in pepper using combined SLAF-seq and BSA
title_full Candidate genes for first flower node identified in pepper using combined SLAF-seq and BSA
title_fullStr Candidate genes for first flower node identified in pepper using combined SLAF-seq and BSA
title_full_unstemmed Candidate genes for first flower node identified in pepper using combined SLAF-seq and BSA
title_short Candidate genes for first flower node identified in pepper using combined SLAF-seq and BSA
title_sort candidate genes for first flower node identified in pepper using combined slaf-seq and bsa
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5860747/
https://www.ncbi.nlm.nih.gov/pubmed/29558466
http://dx.doi.org/10.1371/journal.pone.0194071
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