Lamb F I, Roberts L M, Lord J M
Eur J Biochem. 1985 Apr 15;148(2):265-70. doi: 10.1111/j.1432-1033.1985.tb08834.x.
The primary structure of a precursor protein that contains the toxic (A) and galactose-binding (B) chains of the castor bean lectin, ricin, has been deduced from the nucleotide sequence of cloned DNA complementary to preproricin mRNA. A cDNA library was constructed using maturing castor bean endosperm poly(A)-rich RNA enriched for lectin precursor mRNA by size fractionation. Clones containing lectin mRNA sequences were isolated by hybridization using as a probe a mixture of synthetic oligonucleotides representing all possible sequences for a peptide of the ricin B chain. The entire coding sequence of preproricin was deduced from two overlapping cDNA clones having inserts of 1614 and 1049 base pairs. The coding region (1695 base pairs) consists of a 24-amino-acid N-terminal signal sequence (molecular mass 2836 Da) preceding the A chain 267 amino acids, molecular mass 29 399 Da), which is joined to the B chain (262 amino acids, molecular mass 28 517) by a 12-amino-acid linking region (molecular mass 1385 Da).
已从与前蓖麻毒素mRNA互补的克隆DNA的核苷酸序列中推断出包含蓖麻毒素(一种蓖麻籽凝集素)的毒性(A)链和半乳糖结合(B)链的前体蛋白的一级结构。利用成熟蓖麻籽胚乳中富含聚腺苷酸的RNA构建cDNA文库,该RNA通过大小分级分离法富集凝集素前体mRNA。通过使用代表蓖麻毒素B链肽所有可能序列的合成寡核苷酸混合物作为探针进行杂交,分离出含有凝集素mRNA序列的克隆。前蓖麻毒素的完整编码序列是从两个重叠的cDNA克隆推导出来的,这两个克隆的插入片段分别为1614和1049个碱基对。编码区(1695个碱基对)由A链(267个氨基酸,分子量29399Da)之前的一个24个氨基酸的N端信号序列(分子量2836Da)组成,A链通过一个12个氨基酸的连接区(分子量1385Da)与B链(262个氨基酸,分子量28517Da)相连。