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1.
Genes Cells ; 5(11): 897-903, 2000 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11122377

RESUMO

BACKGROUND: Selenoprotein P is a protein of considerable intrigue, due to its unusual composition and requirements for its biosynthesis. Whereas most selenoproteins contain a single selenocysteine residue, the human, bovine and rodent selenoprotein P genes encode proteins containing 10-12 selenocysteines. Selenoprotein P genes have, to date, only been reported in mammals, and the function of the protein remains elusive. RESULTS: Herein, we report the identification and characterization of nonmammalian selenoprotein P in the zebrafish Danio rerio. Sequencing of the cDNA revealed the presence of 17 selenocysteine codons, the highest number reported in any protein. Two histidine-rich regions present in the mammalian selenoprotein P sequences are conserved in the zebrafish protein, and two SECIS elements are present in the 3' untranslated region. Whole-mount in situ hybridization of zebrafish embryos revealed high levels of expression of selenoprotein P mRNA in fertilized eggs and in the yolk sac of developing embryos. Transient transfection of the cDNA in mammalian cells resulted in efficient expression of the full-length secreted selenoprotein. A single N-glycosylation site is predicted, and shown to be utilized. CONCLUSIONS: Discovery of selenoprotein P in the zebrafish opens a previously unavailable avenue for genetic investigation of the functions of this unusual protein.


Assuntos
Biossíntese de Proteínas , Proteínas/genética , Sequência de Aminoácidos/genética , Animais , Linhagem Celular , Expressão Gênica , Glicosilação , Humanos , Hibridização In Situ , Dados de Sequência Molecular , Especificidade de Órgãos , Mapeamento Físico do Cromossomo , Proteínas/química , RNA Mensageiro/biossíntese , Radioisótopos de Selênio , Selenoproteína P , Selenoproteínas , Análise de Sequência de DNA , Homologia de Sequência de Aminoácidos , Transfecção , Peixe-Zebra , Proteínas de Peixe-Zebra
2.
Development ; 127(14): 3031-44, 2000 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-10862741

RESUMO

Developmental mechanisms underlying traits expressed in larval and adult vertebrates remain largely unknown. Pigment patterns of fishes provide an opportunity to identify genes and cell behaviors required for postembryonic morphogenesis and differentiation. In the zebrafish, Danio rerio, pigment patterns reflect the spatial arrangements of three classes of neural crest-derived pigment cells: black melanocytes, yellow xanthophores and silver iridophores. We show that the D. rerio pigment pattern mutant panther ablates xanthophores in embryos and adults and has defects in the development of the adult pattern of melanocyte stripes. We find that panther corresponds to an orthologue of the c-fms gene, which encodes a type III receptor tyrosine kinase and is the closest known homologue of the previously identified pigment pattern gene, kit. In mouse, fms is essential for the development of macrophage and osteoclast lineages and has not been implicated in neural crest or pigment cell development. In contrast, our analyses demonstrate that fms is expressed and required by D. rerio xanthophore precursors and that fms promotes the normal patterning of melanocyte death and migration during adult stripe formation. Finally, we show that fms is required for the appearance of a late developing, kit-independent subpopulation of adult melanocytes. These findings reveal an unexpected role for fms in pigment pattern development and demonstrate that parallel neural crest-derived pigment cell populations depend on the activities of two essentially paralogous genes, kit and fms.


Assuntos
Melanócitos/fisiologia , Crista Neural/citologia , Peixe-Zebra/genética , Animais , Morte Celular/genética , Movimento Celular/genética , Mapeamento Cromossômico , Clonagem Molecular , Embrião não Mamífero , Regulação da Expressão Gênica no Desenvolvimento , Melanócitos/citologia , Camundongos , Dados de Sequência Molecular , Mutação , Crista Neural/crescimento & desenvolvimento , Proteínas Oncogênicas/genética , Osteoclastos/citologia , Osteoclastos/fisiologia , Proteínas Proto-Oncogênicas c-kit , Pigmentação da Pele/genética , Peixe-Zebra/embriologia , Peixe-Zebra/crescimento & desenvolvimento
5.
Dev Biol ; 197(2): 248-69, 1998 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-9630750

RESUMO

In vertebrates, hematopoietic and vascular progenitors develop from ventral mesoderm. The first primitive wave of hematopoiesis yields embryonic red blood cells, whereas progenitor cells of subsequent definitive waves form all hematopoietic cell lineages. In this report we examine the development of hematopoietic and vasculogenic cells in normal zebrafish and characterize defects in cloche and spadetail mutant embryos. The zebrafish homologs of lmo2, c-myb, fli1, flk1, and flt4 have been cloned and characterized in this study. Expression of these genes identifies embryonic regions that contain hematopoietic and vascular progenitor cells. The expression of c-myb also identifies definitive hematopoietic cells in the ventral wall of the dorsal aorta. Analysis of b316 mutant embryos that carry a deletion of the c-myb gene demonstrates that c-myb is not required for primitive erythropoiesis in zebrafish even though it is expressed in these cells. Both cloche and spadetail mutant embryos have defects in primitive hematopoiesis and definitive hematopoiesis. The cloche mutants also have significant decreases in vascular gene expression, whereas spadetail mutants expressed normal levels of these genes. These studies demonstrate that the molecular mechanisms that regulate hematopoiesis and vasculogenesis have been conserved throughout vertebrate evolution and the clo and spt genes are key regulators of these programs.


Assuntos
Vasos Sanguíneos/embriologia , Hematopoese/genética , Peixe-Zebra/embriologia , Peixe-Zebra/genética , Proteínas Adaptadoras de Transdução de Sinal , Sequência de Aminoácidos , Animais , Sequência de Bases , Primers do DNA/genética , Proteínas de Ligação a DNA/genética , Eritropoese/genética , Evolução Molecular , Regulação da Expressão Gênica no Desenvolvimento , Humanos , Hibridização In Situ , Proteínas com Domínio LIM , Metaloproteínas/genética , Dados de Sequência Molecular , Mutação , Reação em Cadeia da Polimerase , Proteínas Proto-Oncogênicas/genética , Proteínas Proto-Oncogênicas c-myb , Homologia de Sequência de Aminoácidos , Transativadores/genética , Fatores de Transcrição , Proteínas de Peixe-Zebra
6.
Mech Dev ; 67(2): 141-55, 1997 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-9392512

RESUMO

Integrins containing the alpha2 and alpha3 subunits associate with the beta1 subunit to form distinct receptors with partially overlapping adhesive specificities. We report the cloning and sequence of cDNAs that encode the Xenopus orthologues of integrins alpha2 and alpha3 and the expression of these subunits during embryogenesis. Integrin alpha2 and alpha3 mRNAs are first expressed in the dorsal mesoderm and developing notochord at gastrulation. We also show that alpha3 mRNAs are expressed in the entire marginal zone of gastrulae dorsalized with LiCl but that this localization is lost in embryos ventralized by ultraviolet light. Immunoblots reveal that the alpha3 protein is expressed throughout early development, however, the alpha2 protein is not detected until late tailbud stages. Injection of full-length alpha3 transcripts into the animal poles of fertilized eggs results in embryonic defects in paraxial mesoderm attributed to the failure of somites to form segments. Injection of the alpha3 transcripts into the vegetal pole and overexpression of a 5'-truncated alpha3 control construct have no apparent affect on development or somite formation. These data suggest that normal position-specific expression of integrins is important in maintaining the proper organization of tissues during early amphibian morphogenesis.


Assuntos
Antígenos CD/genética , Integrinas/genética , Sequência de Aminoácidos , Animais , Anticorpos/imunologia , Antígenos CD/imunologia , Northern Blotting , Padronização Corporal/genética , Clonagem Molecular , DNA Complementar , Regulação da Expressão Gênica no Desenvolvimento , Humanos , Integrina alfa2 , Integrina alfa3 , Integrinas/imunologia , Dados de Sequência Molecular , Notocorda/metabolismo , RNA Mensageiro/genética , Homologia de Sequência de Aminoácidos , Xenopus laevis/embriologia
7.
Development ; 123: 311-9, 1996 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-9007251

RESUMO

As part of a large scale chemical mutagenesis screen of the zebrafish (Danio rerio) genome, we have identified 33 mutants with defects in hematopoiesis. Complementation analysis placed 32 of these mutants into 17 complementation groups. The allelism of the remaining 1 blood mutant is currently unresolved. We have categorized these blood mutants into four phenotypic classes based on analyses of whole embryos and isolated blood cells, as well as by in situ hybridization using the hematopoietic transcription factors GATA-1 and GATA-2. Embryos mutant for the gene moonshine have few if any proerythroblasts visible on the day circulation begins and normal erythroid cell differentiation is blocked as determined by staining for hemoglobin and GATA-1 expression. Mutations in five genes, chablis, frascati, merlot, retsina, thunderbird and two possibly unique mutations cause a progressive decrease in the number of blood cells during the first 5 days of development. Mutations in another seven genes, chardonnay, chianti, grenache, sauternes, weiflherbst and zinfandel, and two additional mutations result in hypochromic blood cells which also decrease in number as development proceeds. Several of these mutants have immature cells in the circulation, indicating a block in normal erythroid development. The mutation in zinfandel is dominant, and 2-day old heterozygous carriers fail to express detectable levels of hemoglobin and have decreasing numbers of circulating cells during the first 5 days of development. Mutations in two genes, freixenet and yquem, result in the animals that are photosensitive with autofluorescent blood, similar to that found in the human congenital porphyrias. The collection of mutants presented here represent several steps required for normal erythropoiesis. The analysis of these mutants provides a powerful approach towards defining the molecular mechanisms involved in vertebrate hematopoietic development.


Assuntos
Hematopoese/genética , Mutação , Peixe-Zebra/embriologia , Peixe-Zebra/genética , Anemia Hipocrômica/sangue , Anemia Hipocrômica/embriologia , Anemia Hipocrômica/genética , Animais , Embrião não Mamífero/irrigação sanguínea , Contagem de Eritrócitos , Hemoglobinas/metabolismo , Luz/efeitos adversos , Fenótipo , Peixe-Zebra/sangue
8.
Dev Biol ; 160(1): 265-75, 1993 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-7693527

RESUMO

During embryogenesis cells modulate their adhesion to other cells and the surrounding extracellular matrix, in part, through the combination of integrins they express. In order to identify integrins that may mediate morphogenetic cell movements in the early Xenopus embryo, we have used polymerase chain reaction methods to isolate cDNAs encoding Xenopus integrin beta subunits. Based on deduced amino acid sequence, they are identified as homologs of human integrins beta 1, beta 2, beta 3 and beta 6. We also report the cloning and sequencing of cDNAs covering the complete coding region of Xenopus beta 3. Embryonic patterns of expression for these integrin beta subunit mRNAs have been examined both by RNase protection analysis and by whole mount in situ hybridization. In the early embryo the beta 1 subunit is encoded by a maternally transcribed mRNA expressed in all cells, but is most abundant in ectoderm and mesoderm. In contrast, Xenopus beta 3 mRNA is detected in the epidermis, bottle cells of the neural groove, and a subset of cells arising from the ventral blood islands. The beta 2 and beta 6 mRNAs are expressed at high levels in late tailbud stages, although very low levels of beta 6 are also detected in eggs and early embryos. These data provide evidence that multiple integrins are expressed at the earliest stages of vertebrate development coincident with the onset of morphogenesis.


Assuntos
Cadeias beta de Integrinas , Integrinas/genética , Xenopus laevis/embriologia , Sequência de Aminoácidos , Animais , Sequência de Bases , Northern Blotting , Clonagem Molecular , Técnicas de Cultura , DNA , Embrião não Mamífero/metabolismo , Humanos , Integrina beta1 , Integrina beta3 , Integrinas/biossíntese , Dados de Sequência Molecular , Reação em Cadeia da Polimerase , RNA Mensageiro/biossíntese , Mapeamento por Restrição , Homologia de Sequência de Aminoácidos , Xenopus laevis/metabolismo
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