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Cloning and Identification of Porcine SMPX Differentially Expressed in F1 Crossbreds and Their Parents

Cloning and Identification of Porcine SMPX Differentially Expressed in F1 Crossbreds and Their Parents

作     者:Zhu-Qing REN Yuan-Zhu XIONG* Chang-Yan DENG Ming-Gang LEI Agricultural Ministry Key Laboratory of Swine Breeding and Genetics,College of Animal Science and Technology,Huazhong Agricultural University,Wuhan 430070,China Zhu-Qing REN Yuan-Zhu XIONG* Chang-Yan DENG Ming-Gang LEI Agricultural Ministry Key Laboratory of Swine Breeding and Genetics,College of Animal Science and Technology,Huazhong Agricultural University,Wuhan 430070,China

作者机构:Agricultural Ministry Key Laboratory of Swine Breeding and Genetics College of Animal Science and Technology Huazhong Agricultural UniversityWuhan 430070 China 

出 版 物:《Acta Biochimica et Biophysica Sinica》 (生物化学与生物物理学报(英文版))

年 卷 期:2006年第38卷第11期

页      面:753-758页

核心收录:

学科分类:0710[理学-生物学] 0831[工学-生物医学工程(可授工学、理学、医学学位)] 0905[农学-畜牧学] 09[农学] 0703[理学-化学] 

基  金:This work was supported by a grant from the Major State Basic Research Development Program of China (No.G2000016105) 

主  题:skeletal muscle protein pig mRNA differential display expression pattern 

摘      要:In order to investigate porcine heterosis on the molecular basis,Large White (L),a Europeanpurebred,and Meishan (M),a Chinese indigenous purebred,were hybridized directly and reciprocally toproduce F1 hybrids,Large White×Meishan (LM) and Meishan×Large White (ML) *** mRNAdifferential display,we found an expression sequence tag (EST) differentially expressed in F1 hybrids andtheir parents,designated as EST55,which was homologous to human and murine skeletal muscle protein(SMPX),and the full-length cDNA of porcine SMPX was cloned by the rapid amplification of cDNA end(RACE) *** of the mRNA transcript revealed an open reading frame (ORF) of 86 aminoacid residues encoding a nuclear location signal peptide,two overlapping casein kinase Ⅱ phosphorylationsites and one N-glycosylation site with theoretical molecular weight of 9.3 *** analysis revealedthat the deduced protein sequence shared 94%,83% and 78% homology with that of its human,mouse andrat counterparts,*** transcription-polymerase chain reaction (RT-PCR) analysis showedthat it was expressed predominantly in skeletal and heart muscles,whereas at a moderate level in backfat,spleen,stomach and uterus *** single nucleotide polymorphism (SNPs),located in 5′- and 3′-untranslated region (UTR),respectively,were identified by PCR and *** tree and thesecondary structure prediction were also *** possible relationship between porcine SMPX andheterosis was discussed.

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