Sex-biased gene expression during head development in a sexually dimorphic stalk-eyed fly.

Stalk-eyed flies (family Diopsidae) are a model system for studying sexual selection due to the elongated and sexually dimorphic eye-stalks found in many species. These flies are of additional interest because their X chromosome is derived largely from an autosomal arm in other flies. To identify ca...

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Main Authors: Gerald S Wilkinson, Philip M Johns, Jackie D Metheny, Richard H Baker
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3602378?pdf=render
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author Gerald S Wilkinson
Philip M Johns
Jackie D Metheny
Richard H Baker
author_facet Gerald S Wilkinson
Philip M Johns
Jackie D Metheny
Richard H Baker
author_sort Gerald S Wilkinson
collection DOAJ
description Stalk-eyed flies (family Diopsidae) are a model system for studying sexual selection due to the elongated and sexually dimorphic eye-stalks found in many species. These flies are of additional interest because their X chromosome is derived largely from an autosomal arm in other flies. To identify candidate genes required for development of dimorphic eyestalks and investigate how sex-biased expression arose on the novel X, we compared gene expression between males and females using oligonucleotide microarrays and RNA from developing eyestalk tissue or adult heads in the dimorphic diopsid, Teleopsis dalmanni. Microarray analysis revealed sex-biased expression for 26% of 3,748 genes expressed in eye-antennal imaginal discs and concordant sex-biased expression for 86 genes in adult heads. Overall, 415 female-biased and 482 male-biased genes were associated with dimorphic eyestalk development but not differential expression in the adult head. Functional analysis revealed that male-biased genes are disproportionately associated with growth and mitochondrial function while female-biased genes are associated with cell differentiation and patterning or are novel transcripts. With regard to chromosomal effects, dosage compensation occurs by elevated expression of X-linked genes in males. Genes with female-biased expression were more common on the X and less common on autosomes than expected, while male-biased genes exhibited no chromosomal pattern. Rates of protein evolution were lower for female-biased genes but higher for genes that moved on or off the novel X chromosome. These findings cannot be due to meiotic sex chromosome inactivation or by constraints associated with dosage compensation. Instead, they could be consistent with sexual conflict in which female-biased genes on the novel X act primarily to reduce eyespan in females while other genes increase eyespan in both sexes. Additional information on sex-biased gene expression in other tissues and related sexually monomorphic species could confirm this interpretation.
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spelling doaj.art-3f2845734b864cae80869570fc3151412022-12-22T01:58:57ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0183e5982610.1371/journal.pone.0059826Sex-biased gene expression during head development in a sexually dimorphic stalk-eyed fly.Gerald S WilkinsonPhilip M JohnsJackie D MethenyRichard H BakerStalk-eyed flies (family Diopsidae) are a model system for studying sexual selection due to the elongated and sexually dimorphic eye-stalks found in many species. These flies are of additional interest because their X chromosome is derived largely from an autosomal arm in other flies. To identify candidate genes required for development of dimorphic eyestalks and investigate how sex-biased expression arose on the novel X, we compared gene expression between males and females using oligonucleotide microarrays and RNA from developing eyestalk tissue or adult heads in the dimorphic diopsid, Teleopsis dalmanni. Microarray analysis revealed sex-biased expression for 26% of 3,748 genes expressed in eye-antennal imaginal discs and concordant sex-biased expression for 86 genes in adult heads. Overall, 415 female-biased and 482 male-biased genes were associated with dimorphic eyestalk development but not differential expression in the adult head. Functional analysis revealed that male-biased genes are disproportionately associated with growth and mitochondrial function while female-biased genes are associated with cell differentiation and patterning or are novel transcripts. With regard to chromosomal effects, dosage compensation occurs by elevated expression of X-linked genes in males. Genes with female-biased expression were more common on the X and less common on autosomes than expected, while male-biased genes exhibited no chromosomal pattern. Rates of protein evolution were lower for female-biased genes but higher for genes that moved on or off the novel X chromosome. These findings cannot be due to meiotic sex chromosome inactivation or by constraints associated with dosage compensation. Instead, they could be consistent with sexual conflict in which female-biased genes on the novel X act primarily to reduce eyespan in females while other genes increase eyespan in both sexes. Additional information on sex-biased gene expression in other tissues and related sexually monomorphic species could confirm this interpretation.http://europepmc.org/articles/PMC3602378?pdf=render
spellingShingle Gerald S Wilkinson
Philip M Johns
Jackie D Metheny
Richard H Baker
Sex-biased gene expression during head development in a sexually dimorphic stalk-eyed fly.
PLoS ONE
title Sex-biased gene expression during head development in a sexually dimorphic stalk-eyed fly.
title_full Sex-biased gene expression during head development in a sexually dimorphic stalk-eyed fly.
title_fullStr Sex-biased gene expression during head development in a sexually dimorphic stalk-eyed fly.
title_full_unstemmed Sex-biased gene expression during head development in a sexually dimorphic stalk-eyed fly.
title_short Sex-biased gene expression during head development in a sexually dimorphic stalk-eyed fly.
title_sort sex biased gene expression during head development in a sexually dimorphic stalk eyed fly
url http://europepmc.org/articles/PMC3602378?pdf=render
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