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Differential gene expression in liver of inbred chickens and their hybrid offspring
Author(s) -
Sun D.,
Wang D.,
Zhang Y.,
Yu Y.,
Xu G.,
Li J.
Publication year - 2005
Publication title -
animal genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.756
H-Index - 81
eISSN - 1365-2052
pISSN - 0268-9146
DOI - 10.1111/j.1365-2052.2005.01288.x
Subject(s) - heterosis , biology , diallel cross , hybrid , offspring , gene , gene expression , genetics , differential display , zoology , horticulture , pregnancy
Summary Differential display of mRNA was used to analyse the differences of gene expression in liver between chicken hybrids and their parents in a 4 × 4 diallel crosses in order to study the molecular basis of heterosis in chickens. The results indicated that patterns of gene expression in hybrids differ significantly from their parents. Four patterns of differential gene expression were revealed, which included: (i) bands only detected in the hybrid F1s (UNF1); (ii) bands only absent in the hybrid F1s (ABF1); (iii) bands only detected in the parental P1 or P2 lines (UNP1 and UNP2) and (iv) bands absent in the parental P1 or P2 lines (ABP1 and ABP2). In addition, correlations between patterns of gene expression and heterosis percentages of nine carcass traits of 8‐week‐old chickens were evaluated. Statistical results showed that negative correlations between heterosis percentages and the percentage of F1‐specific bands (UNF1) were significant at P < 0.01 for breast muscle yield, leg muscle yield, wing weight, eviscerated weight and eviscerated weight with giblet of 8‐week‐old chickens, and at P < 0.05 for intermuscular fat width. Heterosis percentage was negatively correlated with ABP (bands present in the hybrid F1s and one parental line but absent in the other parental line, ABP1 and ABP2) for breast muscle yield, leg muscle yield, wing weight, eviscerated weight and eviscerated weight with giblet of 8‐week‐old chickens ( P < 0.01). Bands detected only in the hybrid F1s but not in either of the parental lines (UNF 1 ) and bands absent in parental P1 or P2 lines (which includes ABP1 and ABP2) may play important roles in chicken heterosis.