Song Huai-Dong, Sun Xiao-Jian, Deng Min, Zhang Guo-Wei, Zhou Yi, Wu Xin-Yan, Sheng Yan, Chen Yi, Ruan Zheng, Jiang Chun-Lei, Fan Hui-Yong, Zon Leonard I, Kanki John P, Liu Ting Xi, Look A Thomas, Chen Zhu
State Key Lab for Medical Genomics, Shanghai Institute of Hematology, Ruijin Hospital Affiliated to Shanghai Second Medical University, Shanghai 200025, China.
Proc Natl Acad Sci U S A. 2004 Nov 16;101(46):16240-5. doi: 10.1073/pnas.0407241101. Epub 2004 Nov 1.
The zebrafish kidney marrow is considered to be the organ of definitive hematopoiesis, analogous to the mammalian bone marrow. We have sequenced 26,143 ESTs and isolated 304 cDNAs with putative full-length ORF from a zebrafish kidney marrow cDNA library. The ESTs formed 7,742 assemblies, representing both previously identified zebrafish ESTs (56%) and recently discovered zebrafish ESTs (44%). About 30% of these EST assemblies have orthologues in humans, including 1,282 disease-associated genes in the Online Mendelian Inheritance in Man (OMIM) database. Comparison of the effective and regulatory molecules related to erythroid functions across species suggests a good conservation from zebrafish to human. Interestingly, both embryonic and adult zebrafish globin genes showed higher homology to the human embryonic globin genes than to the human fetal/adult ones, consistent with evo-devo correlation hypothesis. In addition, conservation of a whole set of transcription factors involved in globin gene switch suggests the regulatory network for such remodeling mechanism existed before the divergence of the teleost and the ancestor of mammals. We also carried out whole-mount mRNA in situ hybridization assays for 493 cDNAs and identified 80 genes (16%) with tissue-specific expression during the first five days of zebrafish development. Twenty-six of these genes were specifically expressed in hematopoietic or vascular tissues, including three previously unidentified zebrafish genes: coro1a, nephrosin, and dab2. Our results indicate that conserved genetic programs regulate vertebrate hematopoiesis and vasculogenesis, and support the role of the zebrafish as an important animal model for studying both normal development and the molecular pathogenesis of human blood diseases.
斑马鱼的肾脏骨髓被认为是决定性造血的器官,类似于哺乳动物的骨髓。我们对26,143个EST进行了测序,并从斑马鱼肾脏骨髓cDNA文库中分离出304个具有推定全长开放阅读框的cDNA。这些EST形成了7,742个组装体,代表了先前鉴定的斑马鱼EST(56%)和最近发现的斑马鱼EST(44%)。这些EST组装体中约30%在人类中有直系同源物,包括在线人类孟德尔遗传(OMIM)数据库中的1,282个疾病相关基因。跨物种与红细胞功能相关的效应分子和调节分子的比较表明,从斑马鱼到人类具有良好的保守性。有趣的是,斑马鱼的胚胎和成体珠蛋白基因与人类胚胎珠蛋白基因的同源性高于与人类胎儿/成体珠蛋白基因的同源性,这与进化发育相关性假说一致。此外,参与珠蛋白基因转换的一整套转录因子的保守性表明,这种重塑机制的调节网络在硬骨鱼和哺乳动物祖先分化之前就已存在。我们还对493个cDNA进行了全胚胎mRNA原位杂交分析,并鉴定出80个在斑马鱼发育的前五天具有组织特异性表达的基因(16%)。其中26个基因在造血或血管组织中特异性表达,包括三个先前未鉴定的斑马鱼基因:coro1a、nephrosin和dab2。我们的结果表明,保守的遗传程序调节脊椎动物的造血和血管生成,并支持斑马鱼作为研究人类血液疾病正常发育和分子发病机制的重要动物模型的作用。