The evolution of sex-biased gene expression in the Drosophila brain.

Abstract:

:Genes with sex-biased expression in Drosophila are thought to underlie sexually dimorphic phenotypes and have been shown to possess unique evolutionary properties. However, the forces and constraints governing the evolution of sex-biased genes in the somatic tissues of Drosophila are largely unknown. By using population-scale RNA sequencing data, we show that sex-biased genes in the Drosophila brain are highly enriched on the X Chromosome and that most are biased in a species-specific manner. We show that X-linked male-biased genes, and to a lesser extent female-biased genes, are enriched for signatures of directional selection at the gene expression level. By examining the evolutionary properties of gene-flanking regions on the X Chromosome, we find evidence that adaptive cis-regulatory changes are more likely to drive the expression evolution of X-linked male-biased genes than other X-linked genes. Finally, we examine whether constraint owing to broad expression across multiple tissues and genetic constraint owing to the largely shared male and female genomes could be responsible for the observed patterns of gene expression evolution. We find that expression breadth does not constrain the directional evolution of gene expression in the brain. Additionally, we find that the shared genome between males and females imposes a substantial constraint on the expression evolution of sex-biased genes. Overall, these results significantly advance our understanding of the patterns and forces shaping the evolution of sexual dimorphism in the Drosophila brain.

journal_name

Genome Res

journal_title

Genome research

authors

Khodursky S,Svetec N,Durkin SM,Zhao L

doi

10.1101/gr.259069.119

subject

Has Abstract

pub_date

2020-06-01 00:00:00

pages

874-884

issue

6

eissn

1088-9051

issn

1549-5469

pii

gr.259069.119

journal_volume

30

pub_type

杂志文章
  • Gene expression profiling of single cells from archival tissue with laser-capture microdissection and Smart-3SEQ.

    abstract::RNA sequencing (RNA-seq) is a sensitive and accurate method for quantifying gene expression. Small samples or those whose RNA is degraded, such as formalin-fixed paraffin-embedded (FFPE) tissue, remain challenging to study with nonspecialized RNA-seq protocols. Here, we present a new method, Smart-3SEQ, that accuratel...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.234807.118

    authors: Foley JW,Zhu C,Jolivet P,Zhu SX,Lu P,Meaney MJ,West RB

    更新日期:2019-11-01 00:00:00

  • The mouse Aire gene: comparative genomic sequencing, gene organization, and expression.

    abstract::Mutations in the human AIRE gene (hAIRE) result in the development of an autoimmune disease named APECED (autoimmune polyendocrinopathy candidiasis ectodermal dystrophy; OMIM 240300). Previously, we have cloned hAIRE and shown that it codes for a putative transcription-associated factor. Here we report the cloning and...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:

    authors: Blechschmidt K,Schweiger M,Wertz K,Poulson R,Christensen HM,Rosenthal A,Lehrach H,Yaspo ML

    更新日期:1999-02-01 00:00:00

  • The (r)evolution of SINE versus LINE distributions in primate genomes: sex chromosomes are important.

    abstract::The densities of transposable elements (TEs) in the human genome display substantial variation both within individual chromosomes and among chromosome types (autosomes and the two sex chromosomes). Finding an explanation for this variability has been challenging, especially in light of genome landscapes unique to the ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.099044.109

    authors: Kvikstad EM,Makova KD

    更新日期:2010-05-01 00:00:00

  • Strategies for mutational analysis of the large multiexon ATM gene using high-density oligonucleotide arrays.

    abstract::Mutational analysis of large genes with complex genomic structures plays an important role in medical genetics. Technical limitations associated with current mutation screening protocols have placed increased emphasis on the development of new technologies to simplify these procedures. High-density arrays of >90,000-o...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.8.12.1245

    authors: Hacia JG,Sun B,Hunt N,Edgemon K,Mosbrook D,Robbins C,Fodor SP,Tagle DA,Collins FS

    更新日期:1998-12-01 00:00:00

  • Distinct transcription factor complexes act on a permissive chromatin landscape to establish regionalized gene expression in CNS stem cells.

    abstract::Spatially distinct gene expression profiles in neural stem cells (NSCs) are a prerequisite to the formation of neuronal diversity, but how these arise from the regulatory interactions between chromatin accessibility and transcription factor activity has remained unclear. Here, we demonstrate that, despite their distin...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.203513.115

    authors: Hagey DW,Zaouter C,Combeau G,Lendahl MA,Andersson O,Huss M,Muhr J

    更新日期:2016-07-01 00:00:00

  • Identification and analysis of internal promoters in Caenorhabditis elegans operons.

    abstract::The current Caenorhabditis elegans genomic annotation has many genes organized in operons. Using directionally stitched promoterGFP methodology, we have conducted the largest survey to date on the regulatory regions of annotated C. elegans operons and identified 65, over 25% of those studied, with internal promoters. ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.6824707

    authors: Huang P,Pleasance ED,Maydan JS,Hunt-Newbury R,O'Neil NJ,Mah A,Baillie DL,Marra MA,Moerman DG,Jones SJ

    更新日期:2007-10-01 00:00:00

  • Detecting genetic variation in microarray expression data.

    abstract::The use of high-density oligonucleotide arrays to measure the expression levels of thousands of genes in parallel has become commonplace. To take further advantage of the growing body of data, we developed a method, termed "GeSNP," to mine the detailed hybridization patterns in oligonucleotide array expression data fo...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.6307307

    authors: Greenhall JA,Zapala MA,Cáceres M,Libiger O,Barlow C,Schork NJ,Lockhart DJ

    更新日期:2007-08-01 00:00:00

  • Ancestral grass karyotype reconstruction unravels new mechanisms of genome shuffling as a source of plant evolution.

    abstract::The comparison of the chromosome numbers of today's species with common reconstructed paleo-ancestors has led to intense speculation of how chromosomes have been rearranged over time in mammals. However, similar studies in plants with respect to genome evolution as well as molecular mechanisms leading to mosaic synten...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.109744.110

    authors: Murat F,Xu JH,Tannier E,Abrouk M,Guilhot N,Pont C,Messing J,Salse J

    更新日期:2010-11-01 00:00:00

  • Inferring tumor progression from genomic heterogeneity.

    abstract::Cancer progression in humans is difficult to infer because we do not routinely sample patients at multiple stages of their disease. However, heterogeneous breast tumors provide a unique opportunity to study human tumor progression because they still contain evidence of early and intermediate subpopulations in the form...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.099622.109

    authors: Navin N,Krasnitz A,Rodgers L,Cook K,Meth J,Kendall J,Riggs M,Eberling Y,Troge J,Grubor V,Levy D,Lundin P,Månér S,Zetterberg A,Hicks J,Wigler M

    更新日期:2010-01-01 00:00:00

  • The clustering of functionally related genes contributes to CNV-mediated disease.

    abstract::Clusters of functionally related genes can be disrupted by a single copy number variant (CNV). We demonstrate that the simultaneous disruption of multiple functionally related genes is a frequent and significant characteristic of de novo CNVs in patients with developmental disorders (P = 1 × 10(-3)). Using three diffe...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.184325.114

    authors: Andrews T,Honti F,Pfundt R,de Leeuw N,Hehir-Kwa J,Vulto-van Silfhout A,de Vries B,Webber C

    更新日期:2015-06-01 00:00:00

  • Spidey: a tool for mRNA-to-genomic alignments.

    abstract::We have developed a computer program that aligns spliced sequences to genomic sequences, using local alignment algorithms and heuristics to put together a global spliced alignment. Spidey can produce reliable alignments quickly, even when confronted with noise from alternative splicing, polymorphisms, sequencing error...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.195301

    authors: Wheelan SJ,Church DM,Ostell JM

    更新日期:2001-11-01 00:00:00

  • Allele-specific Holliday junction formation: a new mechanism of allelic discrimination for SNP scoring.

    abstract::We report here a new mechanism for allelic discrimination--allele-specific Holliday Junction formation. The Holliday Junction (HJ) is a unique DNA structure that can be formed in a sequence-nonspecific manner by routine PCR. To cause the PCR-based HJ formation to occur in an allele-specific manner, the PCR primers are...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.997703

    authors: Yang Q,Lishanski A,Yang W,Hatcher S,Seet H,Gregg JP

    更新日期:2003-07-01 00:00:00

  • Systematic recovery and analysis of full-ORF human cDNA clones.

    abstract::The Mammalian Gene Collection (MGC) consortium (http://mgc.nci.nih.gov) seeks to establish publicly available collections of full-ORF cDNAs for several organisms of significance to biomedical research, including human. To date over 15,200 human cDNA clones containing full-length open reading frames (ORFs) have been id...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.2473704

    authors: Baross A,Butterfield YS,Coughlin SM,Zeng T,Griffith M,Griffith OL,Petrescu AS,Smailus DE,Khattra J,McDonald HL,McKay SJ,Moksa M,Holt RA,Marra MA

    更新日期:2004-10-01 00:00:00

  • The complete genome and proteome of Mycoplasma mobile.

    abstract::Although often considered "minimal" organisms, mycoplasmas show a wide range of diversity with respect to host environment, phenotypic traits, and pathogenicity. Here we report the complete genomic sequence and proteogenomic map for the piscine mycoplasma Mycoplasma mobile, noted for its robust gliding motility. For t...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.2674004

    authors: Jaffe JD,Stange-Thomann N,Smith C,DeCaprio D,Fisher S,Butler J,Calvo S,Elkins T,FitzGerald MG,Hafez N,Kodira CD,Major J,Wang S,Wilkinson J,Nicol R,Nusbaum C,Birren B,Berg HC,Church GM

    更新日期:2004-08-01 00:00:00

  • Multiplex mapping of chromatin accessibility and DNA methylation within targeted single molecules identifies epigenetic heterogeneity in neural stem cells and glioblastoma.

    abstract::Human tumors are comprised of heterogeneous cell populations that display diverse molecular and phenotypic features. To examine the extent to which epigenetic differences contribute to intratumoral cellular heterogeneity, we have developed a high-throughput method, termed MAPit-patch. The method uses multiplexed ampli...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.161737.113

    authors: Nabilsi NH,Deleyrolle LP,Darst RP,Riva A,Reynolds BA,Kladde MP

    更新日期:2014-02-01 00:00:00

  • Nutritional control of mRNA isoform expression during developmental arrest and recovery in C. elegans.

    abstract::Nutrient availability profoundly influences gene expression. Many animal genes encode multiple transcript isoforms, yet the effect of nutrient availability on transcript isoform expression has not been studied in genome-wide fashion. When Caenorhabditis elegans larvae hatch without food, they arrest development in the...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.133587.111

    authors: Maxwell CS,Antoshechkin I,Kurhanewicz N,Belsky JA,Baugh LR

    更新日期:2012-10-01 00:00:00

  • A large database of chicken bursal ESTs as a resource for the analysis of vertebrate gene function.

    abstract::Chicken B cells create their immunoglobulin repertoire within the Bursa of Fabricius by gene conversion. The high homologous recombination activity is shared by the bursal B-cell-derived DT40 cell line, which integrates transfected DNA constructs at high rates into its endogenous loci. Targeted integration in DT40 is ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.10.12.2062

    authors: Abdrakhmanov I,Lodygin D,Geroth P,Arakawa H,Law A,Plachy J,Korn B,Buerstedde JM

    更新日期:2000-12-01 00:00:00

  • Integrated mapping, chromosomal sequencing and sequence analysis of Cryptosporidium parvum.

    abstract::The apicomplexan Cryptosporidium parvum is one of the most prevalent protozoan parasites of humans. We report the physical mapping of the genome of the Iowa isolate, sequencing and analysis of chromosome 6, and approximately 0.9 Mbp of sequence sampled from the remainder of the genome. To construct a robust physical m...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.1555203

    authors: Bankier AT,Spriggs HF,Fartmann B,Konfortov BA,Madera M,Vogel C,Teichmann SA,Ivens A,Dear PH

    更新日期:2003-08-01 00:00:00

  • Alternative approach to a heavy weight problem.

    abstract::Obesity is reaching epidemic proportions in developed countries and represents a significant risk factor for hypertension, heart disease, diabetes, and dyslipidemia. Splicing mutations constitute at least 14% of disease-causing mutations, thus implicating polymorphisms that affect splicing as likely candidates for dis...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.6661308

    authors: Goren A,Kim E,Amit M,Bochner R,Lev-Maor G,Ahituv N,Ast G

    更新日期:2008-02-01 00:00:00

  • Distal CpG islands can serve as alternative promoters to transcribe genes with silenced proximal promoters.

    abstract::DNA methylation at the promoter of a gene is presumed to render it silent, yet a sizable fraction of genes with methylated proximal promoters exhibit elevated expression. Here, we show, through extensive analysis of the methylome and transcriptome in 34 tissues, that in many such cases, transcription is initiated by a...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.212050.116

    authors: Sarda S,Das A,Vinson C,Hannenhalli S

    更新日期:2017-04-01 00:00:00

  • Large-scale sequencing in human chromosome 12p13: experimental and computational gene structure determination.

    abstract::The detailed genomic organization of a gene-dense region at human chromosome 12p13, spanning 223 kb of contiguous sequence, was determined. This region is composed of 20 genes and several other expressed sequences. Experimental tools including RT-PCR and cDNA sequencing, combined with gene prediction programs, were ut...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.7.3.268

    authors: Ansari-Lari MA,Shen Y,Muzny DM,Lee W,Gibbs RA

    更新日期:1997-03-01 00:00:00

  • Profiling patterned transcripts in Drosophila embryos.

    abstract::Here we describe a high-throughput screen to isolate transcripts with spatially restricted patterns of expression in early embryos. Our approach utilizes robotic automation for rapid analysis of sequence-selected cDNAs in a whole-mount in situ hybridization assay. We determined the spatial distribution of a random col...

    journal_title:Genome research

    pub_type: 信件

    doi:10.1101/gr.84402

    authors: Simin K,Scuderi A,Reamey J,Dunn D,Weiss R,Metherall JE,Letsou A

    更新日期:2002-07-01 00:00:00

  • An analysis of the gene complement of a marsupial, Monodelphis domestica: evolution of lineage-specific genes and giant chromosomes.

    abstract::The newly sequenced genome of Monodelphis domestica not only provides the out-group necessary to better understand our own eutherian lineage, but it enables insights into the innovative biology of metatherians. Here, we compare Monodelphis with Homo sequences from alignments of single nucleotides, genes, and whole chr...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.6093907

    authors: Goodstadt L,Heger A,Webber C,Ponting CP

    更新日期:2007-07-01 00:00:00

  • Mutation scanning by meltMADGE: validations using BRCA1 and LDLR, and demonstration of the potential to identify severe, moderate, silent, rare, and paucimorphic mutations in the general population.

    abstract::We have developed a mutation-scanning approach suitable for whole population screening for unknown mutations. The method, meltMADGE, combines thermal ramp electrophoresis with MADGE to achieve suitable cost efficiency and throughput. The sensitivity was tested in blind trials using 54 amplicons representing the BRCA1 ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.3313405

    authors: Alharbi KK,Aldahmesh MA,Spanakis E,Haddad L,Whittall RA,Chen XH,Rassoulian H,Smith MJ,Sillibourne J,Ball NJ,Graham NJ,Briggs PJ,Simpson IA,Phillips DI,Lawlor DA,Ye S,Humphries SE,Cooper C,Smith GD,Ebrahim S,Eccles

    更新日期:2005-07-01 00:00:00

  • Convergent origination of a Drosophila-like dosage compensation mechanism in a reptile lineage.

    abstract::Sex chromosomes differentiated from different ancestral autosomes in various vertebrate lineages. Here, we trace the functional evolution of the XY Chromosomes of the green anole lizard (Anolis carolinensis), on the basis of extensive high-throughput genome, transcriptome and histone modification sequencing data and r...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.223727.117

    authors: Marin R,Cortez D,Lamanna F,Pradeepa MM,Leushkin E,Julien P,Liechti A,Halbert J,Brüning T,Mössinger K,Trefzer T,Conrad C,Kerver HN,Wade J,Tschopp P,Kaessmann H

    更新日期:2017-12-01 00:00:00

  • Background-suppressed live visualization of genomic loci with an improved CRISPR system based on a split fluorophore.

    abstract::The higher-order structural organization and dynamics of the chromosomes play a central role in gene regulation. To explore this structure-function relationship, it is necessary to directly visualize genomic elements in living cells. Genome imaging based on the CRISPR system is a powerful approach but has limited appl...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.260018.119

    authors: Chaudhary N,Nho SH,Cho H,Gantumur N,Ra JS,Myung K,Kim H

    更新日期:2020-09-01 00:00:00

  • Sequential ChIP-bisulfite sequencing enables direct genome-scale investigation of chromatin and DNA methylation cross-talk.

    abstract::Cross-talk between DNA methylation and histone modifications drives the establishment of composite epigenetic signatures and is traditionally studied using correlative rather than direct approaches. Here, we present sequential ChIP-bisulfite-sequencing (ChIP-BS-seq) as an approach to quantitatively assess DNA methylat...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.133728.111

    authors: Brinkman AB,Gu H,Bartels SJ,Zhang Y,Matarese F,Simmer F,Marks H,Bock C,Gnirke A,Meissner A,Stunnenberg HG

    更新日期:2012-06-01 00:00:00

  • Conservation, regulation, synteny, and introns in a large-scale C. briggsae-C. elegans genomic alignment.

    abstract::A new algorithm, WABA, was developed for doing large-scale alignments between genomic DNA of different species. WABA was used to align 8 million bases of Caenorhabditis briggsae genomic DNA against the entire 97-million-base Caenorhabditis elegans genome. The alignment, including C. briggsae homologs of 154 geneticall...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.10.8.1115

    authors: Kent WJ,Zahler AM

    更新日期:2000-08-01 00:00:00

  • Annotated expressed sequence tags and cDNA microarrays for studies of brain and behavior in the honey bee.

    abstract::To accelerate the molecular analysis of behavior in the honey bee (Apis mellifera), we created expressed sequence tag (EST) and cDNA microarray resources for the bee brain. Over 20,000 cDNA clones were partially sequenced from a normalized (and subsequently subtracted) library generated from adult A. mellifera brains....

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5302

    authors: Whitfield CW,Band MR,Bonaldo MF,Kumar CG,Liu L,Pardinas JR,Robertson HM,Soares MB,Robinson GE

    更新日期:2002-04-01 00:00:00

  • New insulin-like proteins with atypical disulfide bond pattern characterized in Caenorhabditis elegans by comparative sequence analysis and homology modeling.

    abstract::We have identified three new families of insulin homologs in Caenorhabditis elegans. In two of these families, concerted mutations suggest that an additional disulfide bond links B and A domains, and that the A-domain internal disulfide bond is substituted by a hydrophobic interaction. Homology modeling remarkably con...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.8.4.348

    authors: Duret L,Guex N,Peitsch MC,Bairoch A

    更新日期:1998-04-01 00:00:00