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羊驼FGF5基因的分子特征及潜在功能丧失突变的鉴定。

Molecular characterization of the llama FGF5 gene and identification of putative loss of function mutations.

作者信息

Daverio M S, Vidal-Rioja L, Frank E N, Di Rocco F

机构信息

Laboratorio de Genética Molecular, Instituto Multidisciplinario de Biología Celular (IMBICE), CCT CONICET La Plata - CICPBA - UNLP, Calle 526 e/10 y 11, La Plata, 1900, Buenos Aires, Argentina.

IRNASUS, CONICET-UCC Universidad Católica de Córdoba, Av. Armada Argentina 3555, X5014YIG, Cordoba, Argentina.

出版信息

Anim Genet. 2017 Dec;48(6):716-719. doi: 10.1111/age.12616. Epub 2017 Oct 11.

DOI:10.1111/age.12616
PMID:29024003
Abstract

Llama, the most numerous domestic camelid in Argentina, has good fiber-production ability. Although a few genes related to other productive traits have been characterized, the molecular genetic basis of fiber growth control in camelids is still poorly understood. Fibroblast growth factor 5 (FGF5) is a secreted signaling protein that controls hair growth in humans and other mammals. Mutations in the FGF5 gene have been associated with long-hair phenotypes in several species. Here, we sequenced the llama FGF5 gene, which consists of three exons encoding 813 bp. cDNA analysis from hair follicles revealed the expression of two FGF5 alternative spliced transcripts, in one of which exon 2 is absent. DNA variation analysis showed four polymorphisms in the coding region: a synonymous SNP (c.210A>G), a single base deletion (c.348delA), a 12-bp insertion (c.351_352insCATATAACATAG) and a non-sense mutation (c.499C>T). The deletion was always found together with the insertion forming a haplotype and producing a putative truncated protein of 123 amino acids. The c.499C>T mutation also leads to a premature stop codon at position 168. In both cases, critical functional domains of FGF5, including one heparin binding site, are lost. All animals analyzed were homozygous for one of the deleterious mutations or compound heterozygous for both (i.e. c.348delA, c.351_352insCATATAACATAG/c.499T). Sequencing of guanaco samples showed that the FGF5 gene encodes a full-length 270-amino acid protein. These results suggest that FGF5 is likely functional in short-haired wild species and non-functional in the domestic fiber-producing species, the llama.

摘要

羊驼是阿根廷数量最多的家养骆驼科动物,具有良好的纤维生产能力。尽管一些与其他生产性状相关的基因已被鉴定,但骆驼科动物纤维生长控制的分子遗传基础仍知之甚少。成纤维细胞生长因子5(FGF5)是一种分泌型信号蛋白,可控制人类和其他哺乳动物的毛发生长。FGF5基因的突变与多个物种的长毛表型有关。在此,我们对羊驼FGF5基因进行了测序,该基因由三个外显子组成,编码813 bp。毛囊的cDNA分析显示了两种FGF5可变剪接转录本的表达,其中一种缺失外显子2。DNA变异分析显示编码区有四个多态性:一个同义SNP(c.210A>G)、一个单碱基缺失(c.348delA)、一个12 bp插入(c.351_352insCATATAACATAG)和一个无义突变(c.499C>T)。缺失总是与插入一起出现,形成单倍型,并产生一个推定的123个氨基酸的截短蛋白。c.499C>T突变也导致在第168位出现过早的终止密码子。在这两种情况下,FGF5的关键功能域,包括一个肝素结合位点,都丢失了。所有分析的动物对于其中一种有害突变是纯合的,或者对于两者都是复合杂合的(即c.348delA,c.351_352insCATATAACATAG/c.499T)。原驼样本的测序表明,FGF5基因编码一个全长270个氨基酸的蛋白质。这些结果表明,FGF5在短毛野生物种中可能具有功能,而在产纤维的家养物种羊驼中无功能。

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