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31 个大菱鲆全同胞家系的高密度连锁图谱为深入了解整个新精细化基因组组装过程中的重组模式和染色体重排提供了线索。

Highly dense linkage maps from 31 full-sibling families of turbot (Scophthalmus maximus) provide insights into recombination patterns and chromosome rearrangements throughout a newly refined genome assembly.

机构信息

GENEAQUA S.L, 2007 Lugo, Spain.

Departamento de Zoología, Genética y Antropología Física, Facultad de Veterinaria, Universidade de Santiago de Compostela, Lugo, Spain.

出版信息

DNA Res. 2018 Aug 1;25(4):439-450. doi: 10.1093/dnares/dsy015.

DOI:10.1093/dnares/dsy015
PMID:29897548
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6105115/
Abstract

Highly dense linkage maps enable positioning thousands of landmarks useful for anchoring the whole genome and for analysing genome properties. Turbot is the most important cultured flatfish worldwide and breeding programs in the fifth generation of selection are targeted to improve growth rate, obtain disease resistant broodstock and understand sex determination to control sex ratio. Using a Restriction-site Associated DNA approach, we genotyped 18,214 single nucleotide polymorphism in 1,268 turbot individuals from 31 full-sibling families. Individual linkage maps were combined to obtain a male, female and species consensus maps. The turbot consensus map contained 11,845 markers distributed across 22 linkage groups representing a total normalised length of 3,753.9 cM. The turbot genome was anchored to this map, and scaffolds representing 96% of the assembly were ordered and oriented to obtain the expected 22 megascaffolds according to its karyotype. Recombination rate was lower in males, especially around centromeres, and pairwise comparison of 44 individual maps suggested chromosome polymorphism at specific genomic regions. Genome comparison across flatfish provided new evidence on karyotype reorganisations occurring across the evolution of this fish group.

摘要

高密度连锁图谱可定位数千个有用的标记,这些标记可用于锚定整个基因组并分析基因组特性。大菱鲆是世界上最重要的养殖比目鱼,第五代选择育种计划旨在提高生长速度、获得抗疾病的亲鱼,并了解性别决定以控制性别比例。本研究利用基于限制性位点相关的 DNA 标记方法,在 31 个全同胞家系的 1,268 个大菱鲆个体中鉴定了 18,214 个单核苷酸多态性。将个体连锁图谱进行组合,获得了雄性、雌性和种间共识图谱。大菱鲆共识图谱包含 11,845 个标记,分布在 22 个连锁群中,总标准化长度为 3,753.9 cM。将大菱鲆基因组锚定到该图谱上,并对代表组装 96%的支架进行排序和定向,以根据其染色体组型获得预期的 22 个大片段。雄性中的重组率较低,尤其是在着丝粒周围,44 个个体图谱的成对比较表明在特定基因组区域存在染色体多态性。在比目鱼中进行的基因组比较为该鱼类进化过程中发生的染色体重排提供了新的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4deb/6105115/87e1847b8456/dsy015f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4deb/6105115/87e1847b8456/dsy015f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4deb/6105115/87e1847b8456/dsy015f5.jpg

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