Bishop D F, Calhoun D H, Bernstein H S, Hantzopoulos P, Quinn M, Desnick R J
Proc Natl Acad Sci U S A. 1986 Jul;83(13):4859-63. doi: 10.1073/pnas.83.13.4859.
The complete nucleotide sequence has been determined for a lambda gt11 cDNA clone (lambda AG18) containing the full-length coding region for the mature lysosomal form of human alpha-galactosidase A (alpha-Gal A; EC 3.2.1.22). The lambda AG18 insert contained a 1226-base-pair sequence with an open reading frame encoding 398 amino acids of the mature polypeptide (predicted Mr = 45,356) and the last 5 amino acids of the propeptide sequence. The poly(A) signals AATACA and ATTAAA occurred 28 and 11 nucleotides prior to the TAA stop codon, respectively. There was no 3' untranslated region as the poly(A) sequence immediately followed the TAA termination codon; a second independently cloned cDNA confirmed this finding. The predicted amino acid sequence was colinear with 86 nonoverlapping residues (22% of the mature subunit) determined by microsequencing amino-terminal, tryptic, and cyanogen bromide peptides of the purified mature enzyme. Four potential N-glycosylation sites were identified, all of which occurred at predicted beta turns in hydrophilic regions of secondary structure. RNA transfer hybridization analysis of HeLa poly(A)+ RNA demonstrated a single 1.45-kilobase band whose signal was decreased by prior immunoabsorption of polysomes with monospecific alpha-Gal A antibodies. Searches of nucleic acid and protein data bases did not reveal significant homology even with the limited sequences available for mammalian lysosomal enzymes.
已确定一个λgt11 cDNA克隆(λAG18)的完整核苷酸序列,该克隆包含人α-半乳糖苷酶A(α-Gal A;EC 3.2.1.22)成熟溶酶体形式的全长编码区。λAG18插入片段包含一个1226个碱基对的序列,有一个开放阅读框,编码成熟多肽的398个氨基酸(预测的Mr = 45,356)以及前肽序列的最后5个氨基酸。多聚腺苷酸化信号AATACA和ATTAAA分别出现在TAA终止密码子之前的28和11个核苷酸处。由于多聚腺苷酸序列紧跟在TAA终止密码子之后,所以没有3'非翻译区;另一个独立克隆的cDNA证实了这一发现。预测的氨基酸序列与通过对纯化的成熟酶的氨基末端、胰蛋白酶和溴化氰肽进行微量测序确定的86个不重叠残基(成熟亚基的22%)共线。鉴定出四个潜在的N-糖基化位点,所有这些位点都出现在二级结构亲水区预测的β转角处。对HeLa多聚腺苷酸加尾RNA的RNA转移杂交分析显示有一条单一的1.45千碱基条带,其信号在多核糖体先用单特异性α-Gal A抗体进行免疫吸附后减弱。对核酸和蛋白质数据库的搜索未发现明显的同源性,即使与哺乳动物溶酶体酶的有限序列相比也是如此。