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猪过氧化物酶体增殖物激活受体 δ 基因的单倍型与背膘厚有关。

Haplotypes of the porcine peroxisome proliferator-activated receptor delta gene are associated with backfat thickness.

机构信息

Chair of Animal Breeding, Technical University of Munich, Hochfeldweg 1, 85354 Freising - Weihenstephan, Germany.

出版信息

BMC Genet. 2009 Nov 30;10:76. doi: 10.1186/1471-2156-10-76.

Abstract

BACKGROUND

Peroxisome proliferator-activated receptor delta belongs to the nuclear receptor superfamily of ligand-inducible transcription factors. It is a key regulator of lipid metabolism. The peroxisome proliferator-activated receptor delta gene (PPARD) has been assigned to a region on porcine chromosome 7, which harbours a quantitative trait locus for backfat. Thus, PPARD is considered a functional and positional candidate gene for backfat thickness. The purpose of this study was to test this candidate gene hypothesis in a cross of breeds that were highly divergent in lipid deposition characteristics.

RESULTS

Screening for genetic variation in porcine PPARD revealed only silent mutations. Nevertheless, significant associations between PPARD haplotypes and backfat thickness were observed in the F2 generation of the Mangalitsa x Piétrain cross as well as a commercial German Landrace population. Haplotype 5 is associated with increased backfat in F2 Mangalitsa x Piétrain pigs, whereas haplotype 4 is associated with lower backfat thickness in the German Landrace population. Haplotype 4 and 5 carry the same alleles at all but one SNP. Interestingly, the opposite effects of PPARD haplotypes 4 and 5 on backfat thickness are reflected by opposite effects of these two haplotypes on PPAR-delta mRNA levels. Haplotype 4 significantly increases PPAR-delta mRNA levels, whereas haplotype 5 decreases mRNA levels of PPAR-delta.

CONCLUSION

This study provides evidence for an association between PPARD and backfat thickness. The association is substantiated by mRNA quantification. Further studies are required to clarify, whether the observed associations are caused by PPARD or are the result of linkage disequilibrium with a causal variant in a neighbouring gene.

摘要

背景

过氧化物酶体增殖物激活受体 δ 属于配体诱导转录因子的核受体超家族。它是脂质代谢的关键调节因子。过氧化物酶体增殖物激活受体 δ 基因 (PPARD) 已被分配到猪染色体 7 上的一个区域,该区域包含一个背脂的数量性状位点。因此,PPARD 被认为是背脂厚度的功能和位置候选基因。本研究旨在检验该候选基因假说在一个在脂质沉积特征上高度分化的品种杂交中。

结果

在猪 PPARD 中筛选遗传变异仅发现沉默突变。然而,在 Mangalitsa x Piétrain 杂交的 F2 代以及商业德国 Landrace 群体中,PPARD 单倍型与背脂厚度之间存在显著关联。单倍型 5 与 F2 Mangalitsa x Piétrain 猪的背脂增加相关,而单倍型 4 与德国 Landrace 群体的背脂厚度降低相关。单倍型 4 和 5 在除一个 SNP 之外的所有 SNP 上携带相同的等位基因。有趣的是,PPARD 单倍型 4 和 5 对背脂厚度的相反影响反映了这两种单倍型对 PPAR-delta mRNA 水平的相反影响。单倍型 4 显著增加 PPAR-delta mRNA 水平,而单倍型 5 降低 PPAR-delta mRNA 水平。

结论

本研究为 PPARD 与背脂厚度之间的关联提供了证据。这种关联通过 mRNA 定量得到了证实。需要进一步的研究来阐明观察到的关联是由 PPARD 引起的,还是与邻近基因中的因果变异的连锁不平衡造成的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1823/3087513/f600b84a626f/1471-2156-10-76-1.jpg

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