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Development ; 132(16): 3705-15, 2005 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-16077090

RESUMEN

Developmental genetic analysis has shown that embryos of the parasitoid wasp Nasonia vitripennis depend more on zygotic gene products to direct axial patterning than do Drosophila embryos. In Drosophila, anterior axial patterning is largely established by bicoid, a rapidly evolving maternal-effect gene, working with hunchback, which is expressed both maternally and zygotically. Here, we focus on a comparative analysis of Nasonia hunchback function and expression. We find that a lesion in Nasonia hunchback is responsible for the severe zygotic headless mutant phenotype, in which most head structures and the thorax are deleted, as are the three most posterior abdominal segments. This defines a major role for zygotic Nasonia hunchback in anterior patterning, more extensive than the functions described for hunchback in Drosophila or Tribolium. Despite the major zygotic role of Nasonia hunchback, we find that it is strongly expressed maternally, as well as zygotically. Nasonia Hunchback embryonic expression appears to be generally conserved; however, the mRNA expression differs from that of Drosophila hunchback in the early blastoderm. We also find that the maternal hunchback message decays at an earlier developmental stage in Nasonia than in Drosophila, which could reduce the relative influence of maternal products in Nasonia embryos. Finally, we extend the comparisons of Nasonia and Drosophila hunchback mutant phenotypes, and propose that the more severe Nasonia hunchback mutant phenotype may be a consequence of differences in functionally overlapping regulatory circuitry.


Asunto(s)
Tipificación del Cuerpo , Proteínas de Unión al ADN/metabolismo , Proteínas de Drosophila/metabolismo , Proteínas de Insectos/metabolismo , Factores de Transcripción/metabolismo , Avispas , Animales , Secuencia de Bases , Proteínas de Unión al ADN/genética , Proteínas de Drosophila/genética , Regulación del Desarrollo de la Expresión Génica , Ligamiento Genético , Proteínas HMGB/genética , Proteínas HMGB/metabolismo , Hibridación in Situ , Proteínas de Insectos/genética , Datos de Secuencia Molecular , ARN Mensajero Almacenado/metabolismo , Alineación de Secuencia , Factores de Transcripción TCF , Proteína 1 Similar al Factor de Transcripción 7 , Factores de Transcripción/genética , Avispas/anatomía & histología , Avispas/embriología
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