Harris S E, Harris M A, Johnson C M, Bean M F, Dodd J G, Matusik R J, Carr S A, Crabb J W
W. Alton Jones Cell Science Center, Inc., Lake Placid, New York 12946.
J Biol Chem. 1990 Jun 15;265(17):9896-903.
The gene encoding rat seminal vesicle secretion II (SVS II) protein has been cloned from a rat genomic DNA library using a cDNA probe generated from rat dorsal prostate androgen-dependent mRNA. The cloned 7.3-kilobase pair genomic fragment contains approximately 5000 base pairs (bp) of the 5'-flanking region and the entire coding region of the SVS II protein within two exons. A sequence of 4156 bp of the rat SVS II gene has been determined, including 2037 bp of the 5'-flanking region, exon 1 (95 bp), intron 1 (236 bp), exon 2 (1171 bp), and 614 bp of the 3'-flanking region. The 5'-flanking region contains three conserved elements found in other seminal vesicle secretion genes (SVS IV-VI proteins) within 250 bp of the transcription start site as well as a glucocorticoid response element at position -314 in the SVS II gene. The first exon encodes a 22-amino acid leader peptide plus the first 2 amino acids of the secreted protein. The second exon encodes the remaining amino acids in the SVS II protein sequence. The mature protein contains 392 residues and has an Mr of 43,116. Concomitant with the gene analysis, the rat SVS II protein was purified to homogeneity, and 333 residues (85%) of the amino acid sequence were determined by automated Edman degradation. The DNA-deduced sequence and that determined by direct analysis of the protein are in complete agreement. The blocked NH2-terminal amino acid was identified as pyroglutamic acid by mass spectrometry and aminopeptidase digestion. A 13-residue structure with the consensus sequence GSQLKSFGQVKSS is repeated 13 times within the SVS II protein and appears to be involved in the formation of the rat copulatory plug via a transglutaminase reaction cross-linking glutamine and lysine residues. Overall, the SVS II protein sequence exhibits little structural relatedness to any other known protein sequence; however, some similarity can be found between the 13-residue repeat and another repeating structure and apparent transglutaminase substrate in the guinea pig seminal vesicle clotting protein.
利用从大鼠背侧前列腺雄激素依赖性mRNA生成的cDNA探针,已从大鼠基因组DNA文库中克隆出编码大鼠精囊分泌蛋白II(SVS II)的基因。克隆的7.3千碱基对基因组片段包含约5000碱基对(bp)的5'侧翼区以及SVS II蛋白的整个编码区,分布在两个外显子中。已确定大鼠SVS II基因4156 bp的序列,包括2037 bp的5'侧翼区、外显子1(95 bp)、内含子1(236 bp)、外显子2(1171 bp)以及614 bp的3'侧翼区。5'侧翼区在转录起始位点250 bp范围内含有在其他精囊分泌基因(SVS IV - VI蛋白)中发现的三个保守元件,以及SVS II基因中位于 - 314位置的糖皮质激素反应元件。第一个外显子编码一个22个氨基酸的前导肽加上分泌蛋白的前两个氨基酸。第二个外显子编码SVS II蛋白序列中的其余氨基酸。成熟蛋白含有392个残基,Mr为43116。在进行基因分析的同时,大鼠SVS II蛋白被纯化至同质,并且通过自动Edman降解确定了333个残基(85%)的氨基酸序列。DNA推导序列与通过蛋白质直接分析确定的序列完全一致。通过质谱和氨肽酶消化确定封闭的NH2末端氨基酸为焦谷氨酸。一个具有共有序列GSQLKSFGQVKSS的13个残基结构在SVS II蛋白内重复13次,并且似乎通过转谷氨酰胺酶反应交联谷氨酰胺和赖氨酸残基参与大鼠交配栓的形成。总体而言,SVS II蛋白序列与任何其他已知蛋白序列的结构相关性很小;然而,在13个残基重复序列与豚鼠精囊凝血蛋白中的另一个重复结构及明显的转谷氨酰胺酶底物之间可以发现一些相似性。