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1.
Dev Biol ; 403(1): 57-68, 2015 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-25882370

RESUMO

Chromatin insulators orchestrate gene transcription during embryo development and cell differentiation by stabilizing interactions between distant genomic sites. Mutations in genes encoding insulator proteins are generally lethal, making in vivo functional analyses of insulator proteins difficult. In Drosophila, however, mutations in the gene encoding the Suppressor of Hairy wing insulator protein [Su(Hw)] are viable and female sterile, providing an opportunity to study insulator function during oocyte development. Whereas previous reports suggest that the function of Su(Hw) in oogenesis is independent of its insulator activity, many aspects of the role of Su(Hw) in Drosophila oogenesis remain unexplored. Here we show that mutations in su(Hw) result in smaller ring canal lumens and smaller outer ring diameters, which likely obstruct molecular and vesicle passage from nurse cells to the oocyte. Fluorescence microscopy reveals that lack of Su(Hw) leads to excess accumulation of Kelch (Kel) and Filament-actin (F-actin) proteins in the ring canal structures of developing egg chambers. Furthermore, we found that misexpression of the Src oncogene at 64B (Src64B) may cause ring canal development defects as microarray analysis and real-time RT-PCR revealed there is a three fold decrease in Src64B expression in su(Hw) mutant ovaries. Restoration of Src64B expression in su(Hw) mutant female germ cells rescued the ring phenotype but did not restore fertility. We conclude that loss of su(Hw) affects expression of many oogenesis related genes and down-regulates Src64B, resulting in ring canal defects potentially contributing to obstruction of molecular flow and an eventual failure of egg chamber organization.


Assuntos
Proteínas de Drosophila/genética , Drosophila melanogaster/embriologia , Regulação da Expressão Gênica no Desenvolvimento/genética , Oogênese/genética , Proteínas Repressoras/genética , Actinas/metabolismo , Animais , Diferenciação Celular , Proteínas de Drosophila/biossíntese , Proteínas de Drosophila/metabolismo , Feminino , Elementos Isolantes/genética , Proteínas dos Microfilamentos/metabolismo , Ovário/embriologia , Proteínas Tirosina Quinases/biossíntese , Proteínas Proto-Oncogênicas/biossíntese , Proteínas Repressoras/metabolismo
2.
Chromosoma ; 119(2): 177-94, 2010 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-20033198

RESUMO

Chromatin insulators are required for proper temporal and spatial expression of genes in metazoans. Here, we have analyzed the distribution of insulator proteins on the 56F-58A region of chromosome 2R in Drosophila polytene chromosomes to assess the role of chromatin insulators in shaping genome architecture. Data show that the suppressor of Hairy-wing protein [Su(Hw)] is found in three structures differentially associated with insulator proteins: bands, interbands, and multi-gene domains of coexpressed genes. Results show that bands are generally formed by condensation of chromatin that belongs to genes containing one or more Su(Hw) binding sites, whereas, in interbands, Su(Hw) sites appear associated with open chromatin. In addition, clusters of coexpressed genes in this region form bands characterized by the lack of CP190 and BEAF-32 insulator proteins. This pattern correlates with the distribution of specific chromatin marks and is conserved in nurse cells, suggesting that this organization may not be limited to one cell type but represents the basic organization of interphasic chromosomes.


Assuntos
Cromatina , Proteínas de Drosophila/metabolismo , Drosophila melanogaster/genética , Proteínas Repressoras/metabolismo , Animais , Fator de Ligação a CCCTC , Cromatina/química , Cromatina/metabolismo , Proteínas de Ligação a DNA/metabolismo , Drosophila melanogaster/citologia , Drosophila melanogaster/metabolismo , Proteínas do Olho/metabolismo , Regulação da Expressão Gênica , Genoma de Inseto , Elementos Isolantes , Interfase/genética , Proteínas Associadas aos Microtúbulos/metabolismo , Modelos Genéticos , Proteínas Nucleares/metabolismo
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