Inoue K, Takeuchi Y, Takeyama S, Yamaha E, Yamazaki F, Odo S, Harayama S
Kamaishi Laboratories, Marine Biotechnology Institute, Heita Kamaishi, Iwate 026, Japan.
J Mol Evol. 1996 Oct;43(4):348-56. doi: 10.1007/BF02339009.
cDNA encoding the adhesive protein of the mussel Mytilus coruscus (Mcfp1) was isolated. The coding region encoded 848 amino acids (a.a.) comprising the 20-a.a. signal peptide, the 21-a.a. nonrepetitive linker, and the 805-a.a. repetitive domain. Although the first 204 nucleotides and the 3'-untranslated region of Mcfp1 cDNA were homologous to corresponding parts of M. galloprovincialis adhesive protein (Mgfp1) cDNA, the other parts diverged. The representative repeat motif of the repetitive domain, YKPK(I/P)(S/T)YPP(T/S), was similar but slightly different from the repeat motif of Mgfp1. The codon usage patterns for the same amino acids were different in different positions of the decapeptide motif. Almost identical nucleotide sequences encoding the two to 13 repeats appeared several times in the repetitive region, which suggests that the adhesive protein genes of mussels have evolved through the duplication of these repeat units.
分离出了编码贻贝(Mytilus coruscus)粘附蛋白(Mcfp1)的cDNA。编码区编码848个氨基酸,包括20个氨基酸的信号肽、21个氨基酸的非重复连接区和805个氨基酸的重复结构域。尽管Mcfp1 cDNA的前204个核苷酸和3'非翻译区与地中海贻贝(M. galloprovincialis)粘附蛋白(Mgfp1)cDNA的相应部分同源,但其他部分存在差异。重复结构域的代表性重复基序YKPK(I/P)(S/T)YPP(T/S)与Mgfp1的重复基序相似但略有不同。在十肽基序的不同位置,相同氨基酸的密码子使用模式不同。编码2至13个重复序列的几乎相同的核苷酸序列在重复区域中出现了几次,这表明贻贝的粘附蛋白基因是通过这些重复单元的复制进化而来的。