Literature DB >> 24990181

New insights into polar overdominance in callipyge sheep.

C A Bidwell1, J N Waddell, T M Taxis, H Yu, R L Tellam, M K Neary, N E Cockett.   

Abstract

The callipyge phenotype in sheep involves substantial postnatal muscle hypertrophy and other changes to carcass composition. A single nucleotide polymorphism in the DLK1-DIO3 imprinted gene cluster alters gene expression of the paternal allele-specific protein-coding genes and several maternal allele-specific long noncoding RNA and microRNA when the mutation is inherited in cis. The inheritance pattern of the callipyge phenotype is polar overdominant because muscle hypertrophy only occurs in heterozygous animals that inherit a normal maternal allele and the callipyge SNP on the paternal allele (+/C). We examined the changes of gene expression of four major transcripts from the DLK1-DIO3 cluster and four myosin isoforms during the development of muscle hypertrophy in the semimembranosus as well as in the supraspinatus that does not undergo hypertrophy. The homozygous (C/C) animals had an intermediate gene expression pattern for the paternal allele-specific genes and two myosin isoforms, indicating a biological activity that was insufficient to change muscle mass. Transcriptome analysis was conducted by RNA sequencing in the four callipyge genotypes. The data show that homozygous animals (C/C) have lower levels of gene expression at many loci relative to the other three genotypes. A number of the downregulated genes are putative targets of the maternal allele-specific microRNA with gene ontology, indicating regulatory and cell signaling functions. These results suggest that the trans-effect of the maternal noncoding RNA and associated miRNA is to stabilize the expression of a number of regulatory genes at a functional, but low level to make the myofibers of homozygous (C/C) lambs less responsive to hypertrophic stimuli of the paternal allele-specific genes.
© 2014 Stichting International Foundation for Animal Genetics.

Entities:  

Keywords:  DLKzzm3219901; RTLzzm3219901; callipyge sheep; muscle hypertrophy; noncoding RNA; polar overdominance

Mesh:

Substances:

Year:  2014        PMID: 24990181     DOI: 10.1111/age.12132

Source DB:  PubMed          Journal:  Anim Genet        ISSN: 0268-9146            Impact factor:   3.169


  9 in total

1.  Effects and interactions of myostatin and callipyge mutations: I. Growth and carcass traits.

Authors:  Brad A Freking; David A King; Steven D Shackelford; Tommy L Wheeler; Tim P L Smith
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Authors:  Delphine Carouge; Valerie Blanc; Sue E Knoblaugh; Robert J Hunter; Nicholas O Davidson; Joseph H Nadeau
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3.  Methyltransferase-like 21e inhibits 26S proteasome activity to facilitate hypertrophy of type IIb myofibers.

Authors:  Chao Wang; Bin Zhang; Anna C Ratliff; Justine Arrington; Jingjuan Chen; Yan Xiong; Feng Yue; Yaohui Nie; Keping Hu; Wen Jin; W Andy Tao; Christine A Hrycyna; Xiaobo Sun; Shihuan Kuang
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5.  Experimental evaluation does not reveal a direct effect of microRNA from the callipyge locus on DLK1 expression.

Authors:  Huijun Cheng; Xuewen Xu; Tracy Hadfield; Noelle Cockett; Carole Charlier; Michel Georges; Haruko Takeda
Journal:  BMC Genomics       Date:  2014-10-30       Impact factor: 3.969

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Authors:  Tianle Chao; Zhibin Ji; Lei Hou; Jin Wang; Chunlan Zhang; Guizhi Wang; Jianmin Wang
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7.  Identification of genes directly responding to DLK1 signaling in Callipyge sheep.

Authors:  Hui Yu; Jolena N Waddell; Shihuan Kuang; Ross L Tellam; Noelle E Cockett; Christopher A Bidwell
Journal:  BMC Genomics       Date:  2018-04-24       Impact factor: 3.969

Review 8.  A Hearty Dose of Noncoding RNAs: The Imprinted DLK1-DIO3 Locus in Cardiac Development and Disease.

Authors:  Tiffany L Dill; Francisco J Naya
Journal:  J Cardiovasc Dev Dis       Date:  2018-07-10

9.  Candidate genes and gene markers for the resistance to porcine pleuropneumonia.

Authors:  Florian Nietfeld; Doris Höltig; Hermann Willems; Peter Valentin-Weigand; Christine Wurmser; Karl-Heinz Waldmann; Ruedi Fries; Gerald Reiner
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  9 in total

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