Genome-wide identification of meiotic recombination hot spots detected by SLAF in peanut (Arachis hypogaea L.)

Abstract Recombination hot spots (RHP), caused by meiosis, are considered to play crucial roles in improvement and domestication of crop. Cultivated peanut is one of the most important rich-source of oil and protein crops. However, no direct scale of recombination events and RHP have been estimated...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Xiaohua Wang, Ping Xu, Yan Ren, Liang Yin, Shuangling Li, Yan Wang, Yanmao Shi, Hui Li, Xue Cao, Xiaoyuan Chi, Tianyi Yu, Manish K. Pandey, Rajeev K. Varshney, Mei Yuan
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2020
Materias:
R
Q
Acceso en línea:https://doaj.org/article/92dba3bd01d8493f95709476255fb797
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:92dba3bd01d8493f95709476255fb797
record_format dspace
spelling oai:doaj.org-article:92dba3bd01d8493f95709476255fb7972021-12-02T18:50:43ZGenome-wide identification of meiotic recombination hot spots detected by SLAF in peanut (Arachis hypogaea L.)10.1038/s41598-020-70354-x2045-2322https://doaj.org/article/92dba3bd01d8493f95709476255fb7972020-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-020-70354-xhttps://doaj.org/toc/2045-2322Abstract Recombination hot spots (RHP), caused by meiosis, are considered to play crucial roles in improvement and domestication of crop. Cultivated peanut is one of the most important rich-source of oil and protein crops. However, no direct scale of recombination events and RHP have been estimated for peanut. To examine the scale of recombination events and RHP in peanut, a RIL population with 200 lines and a natural population with 49 cultivars were evaluated. The precise integrated map comprises 4837 SLAF markers with genetic length of 2915.46 cM and density of 1.66 markers per cM in whole genome. An average of 30.0 crossover (2.06 cMMb−1) events was detected per RIL plant. The crossover events (CE) showed uneven distribution among B sub-genome (2.32) and A sub-genome (1.85). There were 4.34% and 7.86% of the genome contained large numbers of CE (> 50 cMMb−1) along chromosomes in F6 and natural population, respectively. High density of CE regions called RHP, showed negative relationship to marker haplotypes conservative region but positive to heatmap of recombination. The genes located within the RHP regions by GO categories showed the responding of environmental stimuli, which suggested that recombination plays a crucial role in peanut adaptation to changing environmentsXiaohua WangPing XuYan RenLiang YinShuangling LiYan WangYanmao ShiHui LiXue CaoXiaoyuan ChiTianyi YuManish K. PandeyRajeev K. VarshneyMei YuanNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 10, Iss 1, Pp 1-11 (2020)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Xiaohua Wang
Ping Xu
Yan Ren
Liang Yin
Shuangling Li
Yan Wang
Yanmao Shi
Hui Li
Xue Cao
Xiaoyuan Chi
Tianyi Yu
Manish K. Pandey
Rajeev K. Varshney
Mei Yuan
Genome-wide identification of meiotic recombination hot spots detected by SLAF in peanut (Arachis hypogaea L.)
description Abstract Recombination hot spots (RHP), caused by meiosis, are considered to play crucial roles in improvement and domestication of crop. Cultivated peanut is one of the most important rich-source of oil and protein crops. However, no direct scale of recombination events and RHP have been estimated for peanut. To examine the scale of recombination events and RHP in peanut, a RIL population with 200 lines and a natural population with 49 cultivars were evaluated. The precise integrated map comprises 4837 SLAF markers with genetic length of 2915.46 cM and density of 1.66 markers per cM in whole genome. An average of 30.0 crossover (2.06 cMMb−1) events was detected per RIL plant. The crossover events (CE) showed uneven distribution among B sub-genome (2.32) and A sub-genome (1.85). There were 4.34% and 7.86% of the genome contained large numbers of CE (> 50 cMMb−1) along chromosomes in F6 and natural population, respectively. High density of CE regions called RHP, showed negative relationship to marker haplotypes conservative region but positive to heatmap of recombination. The genes located within the RHP regions by GO categories showed the responding of environmental stimuli, which suggested that recombination plays a crucial role in peanut adaptation to changing environments
format article
author Xiaohua Wang
Ping Xu
Yan Ren
Liang Yin
Shuangling Li
Yan Wang
Yanmao Shi
Hui Li
Xue Cao
Xiaoyuan Chi
Tianyi Yu
Manish K. Pandey
Rajeev K. Varshney
Mei Yuan
author_facet Xiaohua Wang
Ping Xu
Yan Ren
Liang Yin
Shuangling Li
Yan Wang
Yanmao Shi
Hui Li
Xue Cao
Xiaoyuan Chi
Tianyi Yu
Manish K. Pandey
Rajeev K. Varshney
Mei Yuan
author_sort Xiaohua Wang
title Genome-wide identification of meiotic recombination hot spots detected by SLAF in peanut (Arachis hypogaea L.)
title_short Genome-wide identification of meiotic recombination hot spots detected by SLAF in peanut (Arachis hypogaea L.)
title_full Genome-wide identification of meiotic recombination hot spots detected by SLAF in peanut (Arachis hypogaea L.)
title_fullStr Genome-wide identification of meiotic recombination hot spots detected by SLAF in peanut (Arachis hypogaea L.)
title_full_unstemmed Genome-wide identification of meiotic recombination hot spots detected by SLAF in peanut (Arachis hypogaea L.)
title_sort genome-wide identification of meiotic recombination hot spots detected by slaf in peanut (arachis hypogaea l.)
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/92dba3bd01d8493f95709476255fb797
work_keys_str_mv AT xiaohuawang genomewideidentificationofmeioticrecombinationhotspotsdetectedbyslafinpeanutarachishypogaeal
AT pingxu genomewideidentificationofmeioticrecombinationhotspotsdetectedbyslafinpeanutarachishypogaeal
AT yanren genomewideidentificationofmeioticrecombinationhotspotsdetectedbyslafinpeanutarachishypogaeal
AT liangyin genomewideidentificationofmeioticrecombinationhotspotsdetectedbyslafinpeanutarachishypogaeal
AT shuanglingli genomewideidentificationofmeioticrecombinationhotspotsdetectedbyslafinpeanutarachishypogaeal
AT yanwang genomewideidentificationofmeioticrecombinationhotspotsdetectedbyslafinpeanutarachishypogaeal
AT yanmaoshi genomewideidentificationofmeioticrecombinationhotspotsdetectedbyslafinpeanutarachishypogaeal
AT huili genomewideidentificationofmeioticrecombinationhotspotsdetectedbyslafinpeanutarachishypogaeal
AT xuecao genomewideidentificationofmeioticrecombinationhotspotsdetectedbyslafinpeanutarachishypogaeal
AT xiaoyuanchi genomewideidentificationofmeioticrecombinationhotspotsdetectedbyslafinpeanutarachishypogaeal
AT tianyiyu genomewideidentificationofmeioticrecombinationhotspotsdetectedbyslafinpeanutarachishypogaeal
AT manishkpandey genomewideidentificationofmeioticrecombinationhotspotsdetectedbyslafinpeanutarachishypogaeal
AT rajeevkvarshney genomewideidentificationofmeioticrecombinationhotspotsdetectedbyslafinpeanutarachishypogaeal
AT meiyuan genomewideidentificationofmeioticrecombinationhotspotsdetectedbyslafinpeanutarachishypogaeal
_version_ 1718377518700953600