Jiang Yong, Doolittle Russell F
Center for Molecular Genetics, University of California at San Diego, La Jolla, CA 92093-0634, USA.
Proc Natl Acad Sci U S A. 2003 Jun 24;100(13):7527-32. doi: 10.1073/pnas.0932632100. Epub 2003 Jun 13.
The blood coagulation scheme for the puffer fish, Fugu rubripes, has been reconstructed on the basis of orthologs of genes for mammalian blood clotting factors being present in its genome. As expected, clotting follows the same fundamental pattern as has been observed in other vertebrates, even though genes for some clotting factors found in mammals are absent and some others are present in more than one gene copy. All told, 26 different proteins involved in clotting or fibrinolysis were searched against the puffer fish genome. Of these, orthologs were found for 21. Genes for the "contact system" factors (factor XI, factor XII, and prekallikrein) could not be identified. On the other hand, two genes were found for factor IX and four for factor VII. It was evident that not all four factor VII genes are functional, essential active-site residues having been replaced in two of them. A search of the genome of a urochordate, the sea squirt, Ciona intestinalis, did not turn up any genuine orthologs for these 26 factors, although paralogs and/or constituent domains were evident for virtually all of them.
基于河豚(红鳍东方鲀)基因组中存在的哺乳动物血液凝固因子基因的直系同源基因,其血液凝固机制已被重建。不出所料,尽管哺乳动物中发现的一些凝血因子基因缺失,而另一些则以多个基因拷贝的形式存在,但凝血遵循与其他脊椎动物相同的基本模式。总共针对河豚基因组搜索了26种参与凝血或纤维蛋白溶解的不同蛋白质。其中,发现了21种的直系同源基因。未鉴定出“接触系统”因子(因子XI、因子XII和前激肽释放酶)的基因。另一方面,发现了两个因子IX基因和四个因子VII基因。很明显,并非所有四个因子VII基因都具有功能,其中两个基因的必需活性位点残基已被取代。对一种尾索动物海鞘(玻璃海鞘)的基因组进行搜索,未发现这26种因子的任何真正直系同源基因,尽管几乎所有这些因子都存在旁系同源基因和/或组成结构域。