Morgan R O, Jenkins N A, Gilbert D J, Copeland N G, Balsara B R, Testa J R, Fernandez M P
Faculty of Medicine, University of Oviedo, Oviedo, E-33006, Spain.
Genomics. 1999 Aug 15;60(1):40-9. doi: 10.1006/geno.1999.5895.
We have identified and characterized a 12th subfamily of vertebrate annexins by systematic analysis of the primary structure, chromosomal mapping, and molecular evolution of unique cDNA and protein sequences from human and mouse. Distinctive features included rare expression, a codon deletion in conserved repeat 3, and an unusual ablation of the type II calcium-binding sites in tetrad core repeats 1, 3, and 4. The paralogy of novel annexin A10 (following revised nomenclature) was confirmed by FISH-mapping human ANXA10 to chromosome 4q33 and genetic linkage mapping mouse Anxa10 to midchromosome 8. Phylogenetic analysis established that the 5' and 3' halves of the annexin A6 octad are more closely related to annexins A5 and A10, respectively, than they are to each other. Molecular date estimates, paralogy linkage maps between human chromosomes 4 and 5, and annexin structural considerations led to the proposal that annexins A5 and A10 may have been the direct progenitors of annexin A6 octad formation via chromosomal duplication during the genome expansion in early chordates.
通过对来自人类和小鼠的独特cDNA及蛋白质序列的一级结构、染色体定位和分子进化进行系统分析,我们鉴定并表征了脊椎动物膜联蛋白的第12个亚家族。其独特特征包括表达罕见、保守重复序列3中的密码子缺失以及四分体核心重复序列1、3和4中II型钙结合位点的异常缺失。通过荧光原位杂交(FISH)将人类ANXA10定位到染色体4q33以及通过遗传连锁将小鼠Anxa10定位到8号染色体中部,证实了新型膜联蛋白A10(遵循修订后的命名法)的旁系同源性。系统发育分析表明,膜联蛋白A6八联体的5'和3'两半分别与膜联蛋白A5和A10的关系比它们彼此之间的关系更密切。分子年代估计、人类染色体4和5之间的旁系同源连锁图谱以及膜联蛋白结构方面的考虑导致提出这样的观点:在早期脊索动物基因组扩张期间,膜联蛋白A5和A10可能是通过染色体复制形成膜联蛋白A6八联体的直接祖先。