Van Wormhoudt Alain, Sellos Daniel
USMuséum 0401-UMR5178, CNRS/UPMC/MNHN, Département Milieux et Peuplements Aquatiques, Station de Biologie Marine, Muséum National d'Histoire Naturelle, BP 225, 29900 Concarneau, France.
J Mol Evol. 2003 Dec;57(6):659-71. doi: 10.1007/s00239-003-2516-4.
Alpha-amylase from the tropical shrimp Litopenaeus vannamei presents a high degree of polymorphism and at least eight different electromorphs are detected by electrophoresis. Based on nucleotide sequences, three cDNAs have been previously characterized. In this paper we report on the organization and the evolution of corresponding alpha-amylase genes, determined after PCR amplification. Three AMY genes have been characterized, spanning over 3.3 kb and encoding mature proteins of 495 amino acids (aa), which are all expressed in the digestive gland. The existence of nine short introns, ranging from 86 to 454 bp, located at the same positions for each of the different genes, and presenting no similarity between them, is reported. Between 11 and 15% of changes are observed in the coding aa sequences of genes II and III compared to the gene I sequence respectively. One 5' putative promoter sequence has been sequenced and shows no classical TATA box upstream to the coding sequence. Based on the intron size difference, a single PCR (producing the S-R fragments) allows the separation of a partial gene I (750 bp), corresponding to cDNA 20, from the others (650-680 bp). Sequencing different S-R PCR fragments from one shrimp shows at least eight different haplotypes. A complex microsatellite repeat is present in intron 6 of gene II. Using size and sequence differences in this repeated portion, it is possible to characterize two gene subfamilies (IIa and IIb) encoding previously described cDNAs 28 and 37, respectively. For the gene II family, two to four alleles are present in one shrimp corresponding to these two genes. Within the Panama natural population, 35 different alleles are shown at this locus. Regarding alpha-amylase gene structure in the shrimp, many recombinants are present from a set of individuals and constitute an important mechanism of evolution of alpha-amylase function.
来自热带虾凡纳滨对虾的α-淀粉酶呈现出高度多态性,通过电泳可检测到至少八种不同的电泳变体。基于核苷酸序列,先前已鉴定出三个cDNA。在本文中,我们报告了通过PCR扩增后确定的相应α-淀粉酶基因的组织和进化情况。已鉴定出三个AMY基因,跨度超过3.3 kb,编码495个氨基酸(aa)的成熟蛋白,这些蛋白均在消化腺中表达。报告了九个短内含子的存在,其长度在86至454 bp之间,位于每个不同基因的相同位置,且彼此之间没有相似性。与基因I序列相比,分别在基因II和III的编码氨基酸序列中观察到11%至15%的变化。已对一个推定的5'启动子序列进行了测序,结果表明在编码序列上游没有经典的TATA框。基于内含子大小差异,单个PCR(产生S-R片段)可将部分基因I(750 bp,对应于cDNA 20)与其他基因(650 - 680 bp)分离。对一只虾的不同S-R PCR片段进行测序显示至少有八种不同的单倍型。基因II的内含子6中存在一个复杂的微卫星重复序列。利用该重复部分的大小和序列差异,可以鉴定出分别编码先前描述的cDNA 28和37的两个基因亚家族(IIa和IIb)。对于基因II家族,一只虾中对应这两个基因存在两到四个等位基因。在巴拿马自然种群中,该位点显示出35个不同的等位基因。关于虾中α-淀粉酶基因结构,在一组个体中存在许多重组体,它们构成了α-淀粉酶功能进化的重要机制。