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Evo-Devo: the long and winding road.演化发育生物学:漫长而曲折的道路。
Int J Dev Biol. 2003;47(7-8):705-13.
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MLL-SEPTIN6 fusion recurs in novel translocation of chromosomes 3, X, and 11 in infant acute myelomonocytic leukaemia and in t(X;11) in infant acute myeloid leukaemia, and MLL genomic breakpoint in complex MLL-SEPTIN6 rearrangement is a DNA topoisomerase II cleavage site.MLL-SEPTIN6融合在婴儿急性粒单核细胞白血病中3号、X号和11号染色体的新型易位以及婴儿急性髓系白血病的t(X;11)中复发,并且复杂的MLL-SEPTIN6重排中的MLL基因组断点是一个DNA拓扑异构酶II切割位点。
Oncogene. 2002 Jul 11;21(30):4706-14. doi: 10.1038/sj.onc.1205572.
3
Fusion of MLL and MSF in adult de novo acute myelomonocytic leukemia (M4) with t(11;17)(q23;q25).成人新发急性粒单核细胞白血病(M4)伴t(11;17)(q23;q25)中MLL与MSF的融合
Int J Hematol. 2002 Jun;75(5):503-7. doi: 10.1007/BF02982114.
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Evolutionary conservation of zebrafish linkage group 14 with frequently deleted regions of human chromosome 5 in myeloid malignancies.斑马鱼14号连锁群与人类染色体5在髓系恶性肿瘤中频繁缺失区域的进化保守性。
Proc Natl Acad Sci U S A. 2002 Apr 30;99(9):6136-41. doi: 10.1073/pnas.072560099.
5
Organogenesis--heart and blood formation from the zebrafish point of view.器官发生——从斑马鱼视角看心脏与血液形成
Science. 2002 Jan 18;295(5554):457-62. doi: 10.1126/science.1063654.
6
In situ hybridization screen in zebrafish for the selection of genes encoding secreted proteins.在斑马鱼中进行原位杂交筛选以选择编码分泌蛋白的基因。
Dev Dyn. 2001 Dec;222(4):637-44. doi: 10.1002/dvdy.1218.
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A gene expression screen in zebrafish embryogenesis.斑马鱼胚胎发育过程中的基因表达筛选
Genome Res. 2001 Dec;11(12):1979-87. doi: 10.1101/gr.209601.
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Myelopoiesis in the zebrafish, Danio rerio.斑马鱼(Danio rerio)中的髓系造血
Blood. 2001 Aug 1;98(3):643-51. doi: 10.1182/blood.v98.3.643.
9
The human formin-binding protein 17 (FBP17) interacts with sorting nexin, SNX2, and is an MLL-fusion partner in acute myelogeneous leukemia.人类formin结合蛋白17(FBP17)与分选连接蛋白SNX2相互作用,并且是急性髓性白血病中的一种混合谱系白血病(MLL)融合伴侣。
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10
The adaptor molecule Disabled-2 links the transforming growth factor beta receptors to the Smad pathway.衔接分子Disabled-2将转化生长因子β受体与Smad信号通路相连。
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斑马鱼肾脏骨髓中的造血基因表达谱。

Hematopoietic gene expression profile in zebrafish kidney marrow.

作者信息

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

机构信息

State Key Lab for Medical Genomics, Shanghai Institute of Hematology, Ruijin Hospital Affiliated to Shanghai Second Medical University, Shanghai 200025, China.

出版信息

Proc Natl Acad Sci U S A. 2004 Nov 16;101(46):16240-5. doi: 10.1073/pnas.0407241101. Epub 2004 Nov 1.

DOI:10.1073/pnas.0407241101
PMID:15520368
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC528959/
Abstract

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.

摘要

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。