Strong D D, Moore M, Cottrell B A, Bohonus V L, Pontes M, Evans B, Riley M, Doolittle R F
Biochemistry. 1985 Jan 1;24(1):92-101. doi: 10.1021/bi00322a014.
A cDNA library from lamprey liver was constructed in pBR322 and screened with a synthetic mixed oligonucleotide probe, the sequence of which was based on a partial amino acid sequence of the lamprey fibrinogen gamma chain determined by conventional procedures. Among the positive clones was one containing a 600-base insert that covered the carboxy-terminal third of the chain and another with a 1950-base insert that stretched more than full length. The two inserts were sequenced by the Maxam-Gilbert procedure. The DNA sequencing was corroborated by reference to the amino acid sequences of five cyanogen bromide peptides that compose the carboxy-terminal 130 amino acids, as well as to a number of tryptic peptides from elsewhere in the molecule. The clone with the smaller insert (6G) contained 594 nucleotides (not counting G and C tails), 435 of which are coding and correspond to residues 264-408 of the gamma chain. The remaining 159 nucleotides included the terminator codon followed by a noncoding segment. The larger clone (2E) coded for 408 amino acids that could be readily aligned with the 411-residue human gamma chain. A 24-residue signal peptide adjacent to the proposed amino terminal was also inferred. The amino acid sequence of the fibrinogen gamma chain has been differentially conserved during evolution, the lamprey and human sequences being more than 70% identical in certain key regions but dropping to less than 25% in other sections, including the segment thought to be a part of the "coiled coils". Overall, the resemblance amounts to 50% identity. Of the 10 cysteines found in mammalian chains, 9 are at identical positions, but the tenth, which in mammalian fibrinogens is a part of the interdimeric bridging, is absent in the lamprey.
用pBR322构建了七鳃鳗肝脏的cDNA文库,并用合成的混合寡核苷酸探针进行筛选,该探针的序列基于通过常规方法测定的七鳃鳗纤维蛋白原γ链的部分氨基酸序列。在阳性克隆中,一个含有600个碱基的插入片段,覆盖了该链羧基末端的三分之一,另一个含有1950个碱基的插入片段,长度超过全长。通过Maxam-Gilbert方法对这两个插入片段进行了测序。通过参考构成羧基末端130个氨基酸的五个溴化氰肽的氨基酸序列以及分子其他部位的一些胰蛋白酶肽,证实了DNA测序结果。插入片段较小的克隆(6G)包含594个核苷酸(不包括G和C尾),其中435个是编码的,对应于γ链的264-408位残基。其余159个核苷酸包括终止密码子,后面跟着一个非编码片段。较大的克隆(2E)编码408个氨基酸,这些氨基酸可以很容易地与411个残基的人γ链比对。还推断出与推测的氨基末端相邻的一个24个残基的信号肽。纤维蛋白原γ链的氨基酸序列在进化过程中存在差异保守性,七鳃鳗和人类序列在某些关键区域的同一性超过70%,但在其他区域,包括被认为是“卷曲螺旋”一部分的片段,同一性降至不到25%。总体而言,相似性为50%。在哺乳动物链中发现的10个半胱氨酸中,9个处于相同位置,但在七鳃鳗中不存在第十个半胱氨酸,在哺乳动物纤维蛋白原中,它是二聚体间桥接的一部分。