Genome-wide expression analysis of roxarsone-stimulated growth of broiler chickens (Gallus gallus) |
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Authors: | Li Changlu Wang Xiuli Wang Gengyu Wu Changxin Li Ning |
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Affiliation: | aThe State Key Laboratory for Agrobiotechnology, China Agricultural University, Beijing 100094, China;bCollege of Animal Science and Technology, China Agricultural University, Beijing 100094, China |
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Abstract: | Roxarsone is a commonly used additive in chicken (Gallus gallus) industry. However, little is known on the intrinsic molecular mechanism via which the growth performance of birds improves. This study was therefore performed to investigate the expression profiles of genes induced by roxarsone. Fifty-six broiler chickens were divided into two groups, namely treated and untreated with roxarsone. The treated group was provided a diet of 45.4 mg/kg roxarsone medication and the other group acted as control. Data analysis showed that roxarsone consistently and significantly (P < 0.05) increased chicken growth performance. In addition to this a significant (P < 0.05) increase of arsenic residue in liver has been seen. Microarray expression analysis of 8935 genes in liver showed that 22 genes (10 up- and 12 down-regulated) had altered expression throughout the experimental periods. Two novel genes (GenBank accession no. GU724343 and GU724344) were cloned through rapid amplification of cDNA ends (RACE). Gene GU724343 was predicted to encode an unidentified protein and the second gene GU724344 was presumed to encode a new member of immunoglobulin-like receptor (CHIR) family. Our results suggested for the first time that the role of roxarsone could be mainly to modify the expression levels of cell growth, immunity/defense and energy metabolism associated genes, as a result promoting animal growth. Further research on these genes should help to increase the knowledge of improving animal productivity safely and effectively. |
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Keywords: | Abbreviations: aa-dUTP, 5-(3-)-2&prime deoxyuridine-5&prime -triphosphate BSA, bovine serum albumin DMSO, dimethyl sulfoxide GO, gene ontology GSP, gene-specific primers ORF, open reading frame PMT, photomultiplier tube Q-PCR, quantitative PCR RACE, rapid amplification cDNA ends SDS, sodium lauryl sulfate |
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