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Fine mapping of a distal chromosome 4 QTL affecting growth and muscle mass in a chicken advanced intercross line.

Authors :
Lyu S
Arends D
Nassar MK
Brockmann GA
Source :
Animal genetics [Anim Genet] 2017 Jun; Vol. 48 (3), pp. 295-302. Date of Electronic Publication: 2017 Jan 26.
Publication Year :
2017

Abstract

In our previous research, QTL analysis in an F <subscript>2</subscript> cross between the inbred New Hampshire (NHI) and White Leghorn (WL77) lines revealed a growth QTL in the distal part of chromosome 4. To physically reduce the chromosomal interval and the number of potential candidate genes, we performed fine mapping using individuals of generations F <subscript>10</subscript> , F <subscript>11</subscript> and F <subscript>12</subscript> in an advanced intercross line that had been established from the initial F <subscript>2</subscript> mapping population. Using nine single nucleotide polymorphism (SNP) markers within the QTL region for an association analysis with several growth traits from hatch to 20 weeks and body composition traits at 20 weeks, we could reduce the confidence interval from 26.9 to 3.4 Mb. Within the fine mapped region, markers rs14490774, rs314961352 and rs318175270 were in full linkage disequilibrium (D' = 1.0) and showed the strongest effect on growth and muscle mass (LOD ≥ 4.00). This reduced region contains 30 genes, compared to 292 genes in the original region. Chicken 60 K and 600 K SNP chips combined with DNA sequencing of the parental lines were used to call mutations in the reduced region. In the narrowed-down region, 489 sequence variants were detected between NHI and WL77. The most deleterious variants are a missense variant in ADGRA3 (SIFT = 0.02) and a frameshift deletion in the functional unknown gene ENSGALG00000014401 in NHI chicken. In addition, five synonymous variants were discovered in genes PPARGC1A, ADGRA3, PACRGL, SLIT2 and FAM184B. In our study, the confidence interval and the number of potential genes could be reduced 8- and 10- fold respectively. Further research will focus on functional effects of mutant genes.<br /> (© 2017 Stichting International Foundation for Animal Genetics.)

Details

Language :
English
ISSN :
1365-2052
Volume :
48
Issue :
3
Database :
MEDLINE
Journal :
Animal genetics
Publication Type :
Academic Journal
Accession number :
28124378
Full Text :
https://doi.org/10.1111/age.12532