Sellos D, Moal J, Degremont L, Huvet A, Daniel J-Y, Nicoulaud S, Boudry P, Samain J-F, Van Wormhoudt A
Station de Biologie Marine du Muséum National d'Histoire Naturelle, BP 225, 29900 Concarneau, France.
Mar Biotechnol (NY). 2003 Jul-Aug;5(4):360-72. doi: 10.1007/s10126-002-0089-7.
Using the previously determined complementary DNA Sequence of Crassostrea gigas amylase (Y08370), we designed several oligonucleotide primers and used them with polymerase chain reaction (PCR) technology to characterize oyster amylase gene sequences. Two genes encoding 2 different amylases were characterized and sequenced. The 2 genes are similarly organized with 8 exons and 7 introns. Intron insertions are found at the same location in the 2 genes. Sizes and nucleotide sequences are different for the different introns inside each gene and different for the corresponding introns in the 2 genes. Comparing the 2 genes, around 10% of the nucleotides are different along the exons, and comparing the 2 deduced protein sequences, a mean value of 10.4% of amino acids are changed. Genes A and B encode mature proteins of, respectively, 500 and 499 amino acids, which present 94% similarity. A microsatellite (TC(37)) that constitutes the largest part of intron 4 of gene A has been used as a polymorphic marker. A method consisting of a PCR step followed by EcoRI digestion of the obtained fragments was used to observe polymorphism in these 2 genes. Six and 4 alleles for genes A and B, respectively, have been sequenced, leading to a maximum of 2.9% base change. The 2 genes are ubiquitously expressed in the different digestive tissues with quantitative differences. Gene A is strongly expressed in the digestive gland and at a lower level in stomach, while gene B is preferentially expressed in the labial palps. The microsatellite repeat was used in the analysis of 4 populations of Crassostrea gigas from the French Atlantic coast. A high level of polymorphism observed with 30 different alleles of gene A inside the populations should allow their characterization using the mean value of the microsatellite allelic distribution. These populations showed a low level of differentiation ( F(st) between 0 and 0.011); however, the population of Bonne Anse appeared to be distinguished from the other populations.
利用先前测定的太平洋牡蛎淀粉酶(Y08370)的互补DNA序列,我们设计了几种寡核苷酸引物,并将其用于聚合酶链反应(PCR)技术,以鉴定牡蛎淀粉酶基因序列。鉴定并测序了编码两种不同淀粉酶的两个基因。这两个基因的结构相似,均有8个外显子和7个内含子。在这两个基因的相同位置发现了内含子插入。每个基因内不同内含子的大小和核苷酸序列不同,两个基因中相应内含子也不同。比较这两个基因,外显子上约10%的核苷酸不同,比较两个推导的蛋白质序列,平均10.4%的氨基酸发生了变化。基因A和B分别编码由500和499个氨基酸组成的成熟蛋白,它们具有94%的相似性。构成基因A第4内含子最大部分的一个微卫星(TC(37))已被用作多态性标记。一种由PCR步骤和对所得片段进行EcoRI酶切组成的方法被用于观察这两个基因的多态性。分别对基因A和B的6个和4个等位基因进行了测序,导致最大2.9%的碱基变化。这两个基因在不同消化组织中普遍表达,但存在定量差异。基因A在消化腺中强烈表达,在胃中表达水平较低,而基因B优先在唇瓣中表达。该微卫星重复序列被用于分析来自法国大西洋沿岸的4个太平洋牡蛎群体。在群体内部观察到基因A有30个不同等位基因的高水平多态性,这应该可以利用微卫星等位基因分布的平均值对其进行鉴定。这些群体表现出低水平的分化(Fst在0到0.011之间);然而,博讷安斯群体似乎与其他群体不同。