Mapping of QTL on chromosome X for fat deposition, muscling and growth traits in a wild boar x Meishan F sub(2) family using a high-density gene map

Quantitative trait loci (QTL) for fat deposition, growth and muscling traits have been previously mapped on the basis of low-density linkage maps in a wild boar x Meishan F sub(2) family to the chromosome X region flanked by SW2456 and SW1943. Improved QTL resolution was possible using data for F su...

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Bibliographic Details
Published inAnimal genetics Vol. 38; no. 6; pp. 634 - 638
Main Authors Cepica, S, Bartenschlager, H, Geldermann, H
Format Journal Article
LanguageEnglish
Published 01.12.2007
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Summary:Quantitative trait loci (QTL) for fat deposition, growth and muscling traits have been previously mapped on the basis of low-density linkage maps in a wild boar x Meishan F sub(2) family to the chromosome X region flanked by SW2456 and SW1943. Improved QTL resolution was possible using data for F sub(2) animals with a marker density of 2.7 cM distance in the SW2456 to SW1943 region, including AR, SERPINA7 and ACSL4 as candidate genes. The resolution of the QTL scan was increased substantially, as evidenced by the higher F-ratio values for all QTL. Maxima of F-ratio values for fat deposition, muscling and growth traits were 28.6, 18.2 and 16.5 respectively, and those QTL positions accounted for 7.9%, 5.0% and 4.5% of the F sub(2) phenotypic variance (VF sub(2)) respectively. QTL for fatness and growth and for most muscling traits mapped near ACSL4, with the exception of the QTL for ham traits that mapped proximally, in the vicinity of AR. An analysis performed separately for F sub(2) male animals showed the predominant QTL affecting fat deposition traits (up to 13.6% VF sub(2)) near AR and two QTL for muscling traits (up to 9.9% VF sub(2)) mapped close to ACSL4. In the F sub(2) female animals, QTL affecting muscling (up to 12.1% VF sub(2)) mapped at ACSL4 and SW2456, and QTL for fat deposition (10% VF sub(2)) and growth (up to 10.5% VF sub(2)) mapped at ACSL4.
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ISSN:0268-9146
1365-2052
DOI:10.1111/j.1365-2052.2007.01661.x