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利用选择性DNA池定位鸡常染色体上与马立克氏病相关的数量性状基因座区域。

Mapping quantitative trait loci regions associated with Marek's disease on chicken autosomes by means of selective DNA pooling.

作者信息

Lipkin Ehud, Smith Jacqueline, Soller Morris, Burt David W, Fulton Janet E

机构信息

Department of Genetics, The Alexander Silberman Institute of Life Sciences, The Hebrew University of Jerusalem, Edmond J. Safra Campus, Givat Ram, Jerusalem, 91904, Israel.

The Roslin Institute and Royal (Dick) School of Veterinary Studies R(D)SVS, University of Edinburgh, Easter Bush, Midlothian, EH25 9RG, UK.

出版信息

Sci Rep. 2024 Dec 30;14(1):31896. doi: 10.1038/s41598-024-83356-w.

Abstract

Marek's Disease (MD), which can result in neurological damage and tumour formation, has large effects on the economy and animal welfare of the poultry industry worldwide. Previously, we mapped autosomal MD QTL regions (QTLRs) by individual genotyping of an F population from a full-sib advanced intercross line. We further mapped MD QTLRs on the chicken Z chromosome (GGZ) using the same F population, and by selective DNA pooling (SDP) of 8 elite egg production lines. Here we used SDP of the same pools used on GGZ to map autosomal MD QTLRs. Thirty-seven QTLRs were found. Seven of the QTLRs were tested by all sires from the same 8 lines, individually genotyped for QTLR markers. Five of the tested QTLRs were confirmed. Linkage disequilibrium (LD) was calculated for all QTLR markers on the same chromosome, and complex LD blocks were found. Distribution of P and LD values were used to assess the QTLR causative elements. Allele substitution effects were calculated based on both pooled SNP microarray genotypes, and individual genotypes of QTLRs markers. Substantial allele effect and contribution to the phenotypic and genotypic variation were obtained. The results explain part of the MD response, and provide targets for mitigating MD.

摘要

马立克氏病(MD)可导致神经损伤和肿瘤形成,对全球家禽业的经济和动物福利有重大影响。此前,我们通过对全同胞高级杂交系的F群体进行个体基因分型,绘制了常染色体MD数量性状位点区域(QTLR)。我们使用相同的F群体,并通过对8个优质产蛋系进行选择性DNA池化(SDP),进一步绘制了鸡Z染色体(GGZ)上的MD QTLR。在这里,我们使用与GGZ相同的池进行SDP来绘制常染色体MD QTLR。共发现37个QTLR。对来自相同8个系的所有父本进行了QTLR标记的个体基因分型,对其中7个QTLR进行了测试。5个测试的QTLR得到了证实。计算了同一条染色体上所有QTLR标记的连锁不平衡(LD),发现了复杂的LD块。利用P值和LD值的分布来评估QTLR致病元件。基于池化SNP微阵列基因型和QTLR标记的个体基因型计算等位基因替代效应。获得了显著的等位基因效应以及对表型和基因型变异的贡献。这些结果解释了部分MD反应,并为减轻MD提供了靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc51/11686186/5eaa491eeeea/41598_2024_83356_Fig1_HTML.jpg

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