Transcriptomic analysis of genes in the nitrogen recycling pathway of meat‐type chickens divergently selected for feed efficiency

The understanding of the dynamics of ammonia detoxification and excretion in uricotelic species is lagging behind ureotelic species. The relative expression of genes involved in nitrogen recycling and feed efficiency in chickens is unknown. The objective of this study was to investigate the transcri...

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Bibliographic Details
Published inAnimal genetics Vol. 45; no. 2; pp. 215 - 222
Main Authors Aggrey, S. E, Lee, J, Karnuah, A. B, Rekaya, R
Format Journal Article
LanguageEnglish
Published England Blackwell Publishing Ltd 01.04.2014
Wiley Subscription Services, Inc
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Summary:The understanding of the dynamics of ammonia detoxification and excretion in uricotelic species is lagging behind ureotelic species. The relative expression of genes involved in nitrogen recycling and feed efficiency in chickens is unknown. The objective of this study was to investigate the transcriptomics differences in key genes in the nitrogen (N) metabolism and purine biosynthesis pathway in a chicken population divergently selected for low (LRFI) or high (HRFI) residual feed intake at days 35 and 42 using duodenum, liver, pectoralis major (P. major) and kidney. There was a significant positive correlation between RFI and fecal N. The purine salvage pathway was activated in the LRFI compared with HRFI at days 42. The birds in the LRFI population attained greater feed efficiency by having lower FI, increasing their protein retention and producing adequate glutamine to maintain growth compared with the HRFI line. To maintain growth, excess N is deaminated mostly to generate purine nucleotides. Generating purine nucleotides primarily from the purine biosynthesis pathway is energetically costly, and to preserve energy, they preferentially generate nucleotides from the purine salvage pathway. The LRFI birds need to generate sufficient nucleotides to maintain growth despite reduced FI that then results in reduced fecal N.
Bibliography:http://dx.doi.org/10.1111/age.12098
USDA NRI - No. 2009-35205-05208
ArticleID:AGE12098
Table S1 Primer pairs used to analyzed gene expression by quantitative RT-PCR, and size of product.
Georgia Food Industry Partnership - No. 10.26KR696-110
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SourceType-Scholarly Journals-1
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content type line 23
ISSN:0268-9146
1365-2052
DOI:10.1111/age.12098