Single Nucleotide Polymorphisms in Insulin-like Growth Factor 2 (IGF2) gene and their associations with body weight and growth rate traits in indigenous guinea fowls (Numida meleagris) of northern Ghana

Q4 Biochemistry, Genetics and Molecular Biology
Kurukulasuriya Mariesta Jayaroshini Ahiagbe , Christopher Adenyo , Miho Inoue-Murayama , Esinam Nancy Amuzu-Aweh , Patrick Bonney , Boniface Baboreka Kayang
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引用次数: 0

Abstract

Insulin-like Growth Factor 2 (IGF2) plays important roles in stimulating cell proliferation, differentiation and migration culminating its effects as a modulator of juvenile growth in animals. Although the gene that codes for IGF2 (IGF2) has been investigated as a candidate gene in several livestock species, there is no information on polymorphisms in IGF2 in guinea fowls (gIGF2), an important indigenous poultry species from West Africa. Therefore, this study sought to identify the Single Nucleotide Polymorphisms (SNPs) in three populations of indigenous guinea fowls in northern Ghana. Target genomic regions in gIGF2 were amplified and sequenced from 84 indigenous guinea fowls from Upper East Region (n = 17), former Northern Region (n = 22) and Upper West Region (n = 45) of Ghana together with domesticated French variety (n = 3). The sequences were aligned with the reference genomic sequence (domesticated French variety) of chromosome 6 (GenBank accession no., NC_034414.1) to identify SNPs. Statistical associations among the genotypes arising from the SNPs and juvenile growth traits were estimated using linear models. Two novel SNPs were identified in gIGF2 among the indigenous guinea fowls. An insertion of a Guanine (G) within a poly G motif of the intron following the third exon at the 13,955,730 bp location was identified in the majority (84.5%) of indigenous guinea fowls, while the wild type allele was observed in the minority of indigenous guinea fowls and in the domesticated French variety sampled. Also, a biallelic transition arising from the substitution of G by Adenine (A) at position 13,956,496 bp (13,956,496 G > A) located on the fourth exon, which codes for most of the extension peptide of prepro IGF2, was observed in the minority (11.9%) of indigenous guinea fowls. No significant associations among the genotypes arising from the two SNPs, with body weights and weekly growth rates, were identified.

加纳北部土生几内亚鸡(Numida meleagris)胰岛素样生长因子2 (IGF2)基因单核苷酸多态性及其与体重和生长速率性状的关系
胰岛素样生长因子2(IGF2)在刺激细胞增殖、分化和迁移中发挥重要作用,最终作为动物幼年生长的调节剂发挥作用。尽管编码IGF2(IGF2)的基因已被研究为几种牲畜物种的候选基因,但没有关于珍珠鸡(gIGF2)IGF2多态性的信息,珍珠鸡是西非一种重要的本土家禽物种。因此,本研究试图鉴定加纳北部三个土著珍珠鸡种群的单核苷酸多态性(SNPs)。从来自加纳上东部地区(n=17)、前北部地区(n=22)和上西部地区(n=45)的84只本地珍珠鸡以及驯化的法国品种(n=3)中扩增并测序gIGF2的目标基因组区域。将该序列与6号染色体的参考基因组序列(驯化的法国品种)(GenBank登录号,NC_034414.1)进行比对,以鉴定SNPs。使用线性模型估计了SNPs基因型与幼年生长性状之间的统计相关性。在本地珍珠鸡的gIGF2中发现了两个新的SNP。在大多数(84.5%)本土珍珠鸡中发现,在13955730bp位置的第三个外显子之后的内含子的聚G基序中插入了鸟嘌呤(G),而在少数本土珍珠鸟和采样的驯化法国品种中观察到野生型等位基因。此外,在少数(11.9%)本地珍珠鸡中观察到由位于第四外显子上的13956496bp(13956496G>;a)位置的腺嘌呤(a)取代G引起的双等位基因转变,该位置编码IGF2前体的大部分延伸肽。两个SNP产生的基因型与体重和周生长率之间没有显著关联。
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来源期刊
Animal Gene
Animal Gene Agricultural and Biological Sciences-Insect Science
自引率
0.00%
发文量
16
期刊介绍: Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.
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