RNA-Seq Profiling between Commercial and Indigenous Iranian Chickens Highlights Differences in Innate Immune Gene Expression

Author:

Sadr Ayeh Sadat1,Nassiri Mohammadreza23,Ghaderi-Zefrehei Mostafa4,Heidari Maryam5,Smith Jacqueline6ORCID,Muhaghegh Dolatabady Mustafa4

Affiliation:

1. South of Iran Aquaculture Research Institute, Iranian Fisheries Science Research Institute (IFSRI), Agricultural Research Education and Extension Organization (AREEO), Ahvaz 71867-37533, Iran

2. Recombinant Proteins Research Group, The Research Institute of Biotechnology, Ferdowsi University of Mashhad, Mashhad 91779-48974, Iran

3. Research Associate/Peptide Drug and Bioinformatics, School of Biotechnology and Biomolecular Sciences Level 2, E26, University of New South Wales (UNSW), Sydney, NSW 2052, Australia

4. Department of Animal Science, Agricultural Faculty, Yasouj University, Yasouj 75918-74934, Iran

5. Department of Animal Sciences, College of Agriculture, Isfahan University of Technology, Isfahan 83111-84156, Iran

6. The Roslin Institute and Royal (Dick) School of Veterinary Studies, The University of Edinburgh, Easter Bush, Midlothian EH25 9RG, UK

Abstract

The purpose of the current study was to examine transcriptomic-based profiling of differentially expressed innate immune genes between indigenous and commercial chickens. In order to compare the transcriptome profiles of the different chicken breeds, we extracted RNA from blood samples of the Isfahan indigenous chicken (as indigenous) and Ross broiler chicken (as commercial) breeds. RNA-Seq yielded totals of 36,763,939 and 31,545,002 reads for the indigenous and commercial breeds, respectively, with clean reads then aligned to the chicken reference genome (Galgal5). Overall, 1327 genes were significantly differentially expressed, of which 1013 genes were upregulated in the commercial versus the indigenous breed, while 314 were more highly expressed in the indigenous birds. Furthermore, our results demonstrated that the SPARC, ATP6V0D2, IL4I1, SMPDL3A, ADAM7, TMCC3, ULK2, MYO6, THG1L and IRG1 genes were the most significantly expressed genes in the commercial birds and the PAPPA, DUSP1, PSMD12, LHX8, IL8, TRPM2, GDAP1L1, FAM161A, ABCC2 and ASAH2 genes were the most significant in the indigenous chickens. Of notable finding in this study was that the high-level gene expressions of heat-shock proteins (HSPs) in the indigenous breeds could serve as a guideline for future genetic improvement. This study identified genes with breed-specific expression, and comparative transcriptome analysis helped understanding of the differences in underlying genetic mechanisms between commercial and local breeds. Therefore, the current results can be used to identify candidate genes for further breed improvement.

Funder

Biotechnology and Biological Sciences Research Council

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

Reference50 articles.

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