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Drosophila RNA polymerase III repressor Maf1 controls body size and developmental timing by modulating tRNAiMet synthesis and systemic insulin signaling
by
Grewal, Savraj S
, Rideout, Elizabeth J
, Marshall, Lynne
in
Animals
/ Biological Sciences
/ Blotting, Western
/ Body size
/ Body Size - physiology
/ Cloning, Molecular
/ Dimethyl Sulfoxide - pharmacology
/ DNA Primers - genetics
/ DNA-directed RNA polymerase
/ Drosophila
/ Drosophila - growth & development
/ Drosophila - metabolism
/ Drosophila Proteins - genetics
/ Drosophila Proteins - metabolism
/ Fat body
/ Flow Cytometry
/ Insect Proteins - metabolism
/ Insulin
/ Insulin - metabolism
/ Larva - metabolism
/ larvae
/ larval development
/ Metazoa
/ Methionine
/ Nutrient availability
/ Nutrients
/ peptides
/ phenotype
/ Polyribosomes - metabolism
/ Real-Time Polymerase Chain Reaction
/ Repressor Proteins - genetics
/ Repressor Proteins - metabolism
/ Repressors
/ RNA Polymerase III - metabolism
/ RNA, Transfer, Met - biosynthesis
/ Signal transduction
/ Signal Transduction - physiology
/ Sirolimus - pharmacology
/ Transcription
/ transfer RNA
/ tRNA
2012
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Drosophila RNA polymerase III repressor Maf1 controls body size and developmental timing by modulating tRNAiMet synthesis and systemic insulin signaling
by
Grewal, Savraj S
, Rideout, Elizabeth J
, Marshall, Lynne
in
Animals
/ Biological Sciences
/ Blotting, Western
/ Body size
/ Body Size - physiology
/ Cloning, Molecular
/ Dimethyl Sulfoxide - pharmacology
/ DNA Primers - genetics
/ DNA-directed RNA polymerase
/ Drosophila
/ Drosophila - growth & development
/ Drosophila - metabolism
/ Drosophila Proteins - genetics
/ Drosophila Proteins - metabolism
/ Fat body
/ Flow Cytometry
/ Insect Proteins - metabolism
/ Insulin
/ Insulin - metabolism
/ Larva - metabolism
/ larvae
/ larval development
/ Metazoa
/ Methionine
/ Nutrient availability
/ Nutrients
/ peptides
/ phenotype
/ Polyribosomes - metabolism
/ Real-Time Polymerase Chain Reaction
/ Repressor Proteins - genetics
/ Repressor Proteins - metabolism
/ Repressors
/ RNA Polymerase III - metabolism
/ RNA, Transfer, Met - biosynthesis
/ Signal transduction
/ Signal Transduction - physiology
/ Sirolimus - pharmacology
/ Transcription
/ transfer RNA
/ tRNA
2012
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Drosophila RNA polymerase III repressor Maf1 controls body size and developmental timing by modulating tRNAiMet synthesis and systemic insulin signaling
by
Grewal, Savraj S
, Rideout, Elizabeth J
, Marshall, Lynne
in
Animals
/ Biological Sciences
/ Blotting, Western
/ Body size
/ Body Size - physiology
/ Cloning, Molecular
/ Dimethyl Sulfoxide - pharmacology
/ DNA Primers - genetics
/ DNA-directed RNA polymerase
/ Drosophila
/ Drosophila - growth & development
/ Drosophila - metabolism
/ Drosophila Proteins - genetics
/ Drosophila Proteins - metabolism
/ Fat body
/ Flow Cytometry
/ Insect Proteins - metabolism
/ Insulin
/ Insulin - metabolism
/ Larva - metabolism
/ larvae
/ larval development
/ Metazoa
/ Methionine
/ Nutrient availability
/ Nutrients
/ peptides
/ phenotype
/ Polyribosomes - metabolism
/ Real-Time Polymerase Chain Reaction
/ Repressor Proteins - genetics
/ Repressor Proteins - metabolism
/ Repressors
/ RNA Polymerase III - metabolism
/ RNA, Transfer, Met - biosynthesis
/ Signal transduction
/ Signal Transduction - physiology
/ Sirolimus - pharmacology
/ Transcription
/ transfer RNA
/ tRNA
2012
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Drosophila RNA polymerase III repressor Maf1 controls body size and developmental timing by modulating tRNAiMet synthesis and systemic insulin signaling
Journal Article
Drosophila RNA polymerase III repressor Maf1 controls body size and developmental timing by modulating tRNAiMet synthesis and systemic insulin signaling
2012
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Overview
The target-of-rapamycin pathway couples nutrient availability with tissue and organismal growth in metazoans. The key effectors underlying this growth are, however, unclear. Here we show that Maf1, a repressor of RNA polymerase III-dependent tRNA transcription, is an important mediator of nutrient-dependent growth in DROSOPHILA: We find nutrients promote tRNA synthesis during larval development by inhibiting Maf1. Genetic inhibition of Maf1 accelerates development and increases body size. These phenotypes are due to a non–cell-autonomous effect of Maf1 inhibition in the fat body, the main larval endocrine organ. Inhibiting Maf1 in the fat body increases growth by promoting the expression of brain-derived insulin-like peptides and consequently enhanced systemic insulin signaling. Remarkably, the effects of Maf1 inhibition are reproduced in flies carrying one extra copy of the initiator methionine tRNA, tRNAiMet. These findings suggest the stimulation of tRNAiMet synthesis via inhibition of dMaf1 is limiting for nutrition-dependent growth during development.
Publisher
National Academy of Sciences,National Acad Sciences
Subject
/ Dimethyl Sulfoxide - pharmacology
/ Drosophila - growth & development
/ Drosophila Proteins - genetics
/ Drosophila Proteins - metabolism
/ Fat body
/ Insect Proteins - metabolism
/ Insulin
/ larvae
/ Metazoa
/ peptides
/ Real-Time Polymerase Chain Reaction
/ Repressor Proteins - genetics
/ Repressor Proteins - metabolism
/ RNA Polymerase III - metabolism
/ RNA, Transfer, Met - biosynthesis
/ Signal Transduction - physiology
/ tRNA
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