Male-specific fruitless isoforms target neurodevelopmental genes to specify a sexually dimorphic nervous system
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In: Current Biology, Vol. 24, No. 3, 03.02.2014, p. 229-41.
Research output: Contribution to journal › Article › peer-review
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T1 - Male-specific fruitless isoforms target neurodevelopmental genes to specify a sexually dimorphic nervous system
AU - Neville, Megan C
AU - Nojima, Tetsuya
AU - Ashley, Elizabeth
AU - Parker, Darren J
AU - Walker, John
AU - Southall, Tony
AU - Van de Sande, Bram
AU - Marques, Ana C
AU - Fischer, Bettina
AU - Brand, Andrea H
AU - Russell, Steven
AU - Ritchie, Michael G
AU - Aerts, Stein
AU - Goodwin, Stephen F
N1 - Copyright © 2014 The Authors. Published by Elsevier Inc. All rights reserved.
PY - 2014/2/3
Y1 - 2014/2/3
N2 - BACKGROUND: In Drosophila, male courtship behavior is regulated in large part by the gene fruitless (fru). fru encodes a set of putative transcription factors that promote male sexual behavior by controlling the development of sexually dimorphic neuronal circuitry. Little is known about how Fru proteins function at the level of transcriptional regulation or the role that isoform diversity plays in the formation of a male-specific nervous system.RESULTS: To characterize the roles of sex-specific Fru isoforms in specifying male behavior, we generated novel isoform-specific mutants and used a genomic approach to identify direct Fru isoform targets during development. We demonstrate that all Fru isoforms directly target genes involved in the development of the nervous system, with individual isoforms exhibiting unique binding specificities. We observe that fru behavioral phenotypes are specified by either a single isoform or a combination of isoforms. Finally, we illustrate the utility of these data for the identification of novel sexually dimorphic genomic enhancers and novel downstream regulators of male sexual behavior.CONCLUSIONS: These findings suggest that Fru isoform diversity facilitates both redundancy and specificity in gene expression, and that the regulation of neuronal developmental genes may be the most ancient and conserved role of fru in the specification of a male-specific nervous system.
AB - BACKGROUND: In Drosophila, male courtship behavior is regulated in large part by the gene fruitless (fru). fru encodes a set of putative transcription factors that promote male sexual behavior by controlling the development of sexually dimorphic neuronal circuitry. Little is known about how Fru proteins function at the level of transcriptional regulation or the role that isoform diversity plays in the formation of a male-specific nervous system.RESULTS: To characterize the roles of sex-specific Fru isoforms in specifying male behavior, we generated novel isoform-specific mutants and used a genomic approach to identify direct Fru isoform targets during development. We demonstrate that all Fru isoforms directly target genes involved in the development of the nervous system, with individual isoforms exhibiting unique binding specificities. We observe that fru behavioral phenotypes are specified by either a single isoform or a combination of isoforms. Finally, we illustrate the utility of these data for the identification of novel sexually dimorphic genomic enhancers and novel downstream regulators of male sexual behavior.CONCLUSIONS: These findings suggest that Fru isoform diversity facilitates both redundancy and specificity in gene expression, and that the regulation of neuronal developmental genes may be the most ancient and conserved role of fru in the specification of a male-specific nervous system.
KW - Animals
KW - Base Sequence
KW - Central Nervous System/metabolism
KW - Drosophila Proteins/genetics
KW - Drosophila melanogaster/genetics
KW - Gene Expression Regulation, Developmental/genetics
KW - Gene Knockout Techniques
KW - Male
KW - Molecular Sequence Data
KW - Nerve Tissue Proteins/genetics
KW - Neurogenesis/genetics
KW - Protein Isoforms/genetics
KW - Sex Characteristics
KW - Sexual Behavior, Animal/physiology
KW - Transcription Factors/genetics
U2 - 10.1016/j.cub.2013.11.035
DO - 10.1016/j.cub.2013.11.035
M3 - Article
C2 - 24440396
VL - 24
SP - 229
EP - 241
JO - Current Biology
JF - Current Biology
SN - 0960-9822
IS - 3
ER -