Polysomal and postpolysomal mRNA were prepared from Drosophila egg chambers or embryos of different developmental stages. Cell-free translation of these mRNA followed by 2-dimensional gel electrophoresis of the products indicated the presence of a specific mRNA that appears to be translated (polysome-associated) during oogenesis. This mRNA, designated T1 mRNA, is selectively excluded from polysomes in 3-h- and 5-h-old embryos and is again translated in 18-h-old embryos. A clone containing DNA complementary to T1 mRNA was selected from a library of recombinant DNA prepared from polyadenylylated ovary RNA. This clone was positively identified by hybrid-selected translation followed by 2-dimensional gel electrophoresis and autoradiography. T1 mRNA is polyadenylylated and codes for a small, acidic protein. The cloned probe hybridizes to a unique site (2L-39CD) of the polytene chromosomes, very close to the histone genes. This mRNA probably is under specific translational regulation in contrast to a background of a large number of other abundant mRNA that are translated at all developmental stages examined.

TRANSLATIONAL REGULATION OF A SPECIFIC GENE DURING OOGENESIS AND EMBRYOGENESIS OF DROSOPHILA-MELANOGASTER

FRUSCOLONI P;
1983

Abstract

Polysomal and postpolysomal mRNA were prepared from Drosophila egg chambers or embryos of different developmental stages. Cell-free translation of these mRNA followed by 2-dimensional gel electrophoresis of the products indicated the presence of a specific mRNA that appears to be translated (polysome-associated) during oogenesis. This mRNA, designated T1 mRNA, is selectively excluded from polysomes in 3-h- and 5-h-old embryos and is again translated in 18-h-old embryos. A clone containing DNA complementary to T1 mRNA was selected from a library of recombinant DNA prepared from polyadenylylated ovary RNA. This clone was positively identified by hybrid-selected translation followed by 2-dimensional gel electrophoresis and autoradiography. T1 mRNA is polyadenylylated and codes for a small, acidic protein. The cloned probe hybridizes to a unique site (2L-39CD) of the polytene chromosomes, very close to the histone genes. This mRNA probably is under specific translational regulation in contrast to a background of a large number of other abundant mRNA that are translated at all developmental stages examined.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/293932
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