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1.
Dev Biol ; 276(1): 47-63, 2004 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-15531363

RESUMO

XHRT1 is a member of the HRT/Hey protein subfamily that are known as Notch effectors. XHRT1 is expressed in the developing floor plate and encodes a basic helix-loop-helix (bHLH) transcription repressor. Here, we show that XHRT1 misexpression in the neural plate inhibits differentiation of neural precursor cells and thus may be important for floor plate cells to prevent them from adopting a neuronal fate. Deletion analysis indicated that inhibition of differentiation by XHRT1 requires the DNA-binding bHLH motif and either the Orange domain or the C-terminal region. XHRT1 could efficiently homodimerize and heterodimerize with hairy proteins. Among those hairy genes, Xhairy2b shows extensive overlap of expression with XHRT1 in floor plate precursors and may be a biologically relevant XHRT1 partner. Dimerization is mediated through both the bHLH and downstream sequences, the Orange domain being particularly important for the efficiency of the interaction. Using chimeric constructs between XHRT1 and the ESR9 bHLH-O protein that does not interact with Xhairy1 and Xhairy2b, we found that both the bHLH domain and downstream sequences of XHRT1 were required for heterodimerization with Xhairy2b, while only the XHRT1 sequences downstream of the Orange domain are required for the interaction with Xhairy1. Together, these results suggest that XHRT1 plays a role in floor plate cell development and highlight the importance of the Orange and downstream sequences in dimerization and in the selection of the bHLH partners.


Assuntos
Proteínas de Ligação a DNA/metabolismo , Regulação da Expressão Gênica no Desenvolvimento , Seleção Genética , Fatores de Transcrição/metabolismo , Proteínas de Xenopus/metabolismo , Sequência de Aminoácidos , Animais , Fatores de Transcrição Hélice-Alça-Hélice Básicos , Proteínas de Ligação a DNA/genética , Dimerização , Ensaio de Desvio de Mobilidade Eletroforética , Embrião não Mamífero , Genes Reporter , Células HeLa , Humanos , Hibridização In Situ , Luciferases/metabolismo , Microinjeções , Neurônios/citologia , Testes de Precipitina , Estrutura Terciária de Proteína , Deleção de Sequência , Células-Tronco/citologia , Fatores de Transcrição/química , Fatores de Transcrição/genética , Transcrição Gênica , Tubulina (Proteína)/metabolismo , Técnicas do Sistema de Duplo-Híbrido , Xenopus , Proteínas de Xenopus/química , Proteínas de Xenopus/genética
2.
Dev Dyn ; 228(4): 716-25, 2003 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-14648848

RESUMO

Hairy-related transcription factor (HRT/Hey) genes encode a novel subfamily of basic helix-loop-helix (bHLH) transcription factors related to the Drosophila hairy and Enhancer-of-split (E(spl)) and the mammalian HES proteins that function as downstream mediators of Notch signaling. Using the yeast two-hybrid approach, a previously uncharacterized protein was identified in Xenopus that interacts with XHRT1 (originally referred to as bc8), one member of the HRT/Hey subclass. This protein is evolutionarily conserved in chordates. It binds to sequences adjacent to the bHLH domain of XHRT1 known as the Orange domain and has been named bc8 Orange interacting protein (BOIP). BOIP shows a rather uniform subcellular localization and is recruited to the nucleus upon binding to XHRT1. In Xenopus, XBOIP mRNA is detected by RNase protection analysis throughout embryogenesis. In the adult, the strongest expression is detected in testis. In the mouse, high levels of BOIP mRNA are also found in adult testis. No expression is detected in the embryo and in any of the other adult organs tested. In situ hybridization revealed that BOIP transcripts were detected almost exclusively in round spermatids and that this expression overlaps with that of Hey1 (HRT1), which is expressed throughout spermatogenesis. In view of the importance of the Orange domain for HRT/Hey function, the newly identified BOIP proteins may serve as regulators specifically of HRT1/Hey1 activity.


Assuntos
Proteínas de Transporte/biossíntese , Proteínas de Transporte/genética , Proteínas de Ciclo Celular/química , DNA Complementar/metabolismo , Regulação da Expressão Gênica no Desenvolvimento , Espermatogênese , Espermatozoides/metabolismo , Sequência de Aminoácidos , Animais , Fatores de Transcrição Hélice-Alça-Hélice Básicos , Proteínas de Ciclo Celular/metabolismo , Clonagem Molecular , Sequência Conservada , Embrião de Mamíferos/metabolismo , Embrião não Mamífero , Biblioteca Gênica , Células HeLa , Humanos , Imuno-Histoquímica , Hibridização In Situ , Luciferases/metabolismo , Masculino , Proteínas de Membrana/metabolismo , Camundongos , Dados de Sequência Molecular , Proteínas Nucleares/biossíntese , Proteínas Nucleares/genética , Plasmídeos/metabolismo , Testes de Precipitina , Ligação Proteica , Estrutura Terciária de Proteína , RNA/metabolismo , RNA Mensageiro/metabolismo , Receptores Notch , Ribonucleases/metabolismo , Homologia de Sequência de Aminoácidos , Transdução de Sinais , Testículo/metabolismo , Transfecção , Técnicas do Sistema de Duplo-Híbrido , Xenopus
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