Evidence map›Paper›PMID 27414415›Full record

ArticlePLoS genetics2016

Expansion of GA Dinucleotide Repeats Increases the Density of CLAMP Binding Sites on the X-Chromosome to Promote Drosophila Dosage Compensation.

Guray Kuzu, Emily G Kaye, Jessica Chery, Trevor Siggers, Lin Yang, Jason R Dobson, Sonia Boor, Jacob Bliss, Wei Liu, Gerwald Jogl and 5 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.9field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 63 citations in OpenAlex.

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  12. Sequence reliance of abioRxiv : the preprint server for biology · 2023
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  13. Review
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  15. Dosage Compensation inInternational journal of molecular sciences · 2022
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 8 institutions in 2 countries.

Guray KuzuDepartment of Molecular Biology, Cellular Biology and Biochemistry, Brown University, Providence, Rhode Island, United States of America.ORCID 0000-0002-7910-5985
Emily G KayeDepartment of Molecular Biology, Cellular Biology and Biochemistry, Brown University, Providence, Rhode Island, United States of America.
Jessica CheryDepartment of Cell Biology, Massachusetts General Hospital Cancer Center, Boston, Massachusetts, United States of America.
Trevor SiggersDepartment of Biology, Boston University, Boston, Massachusetts, United States of America.
Lin YangMolecular and Computational Biology Program, Department of Biological Sciences, University of Southern California, Los Angeles, California, United States of America.ORCID 0000-0001-9155-6386
Jason R DobsonNovartis Institutes for Biomedical Research, Cambridge, Massachusetts, United States of America.ORCID 0000-0002-2306-2250
Sonia BoorDepartment of Molecular Biology, Cellular Biology and Biochemistry, Brown University, Providence, Rhode Island, United States of America.
Jacob BlissDepartment of Molecular Biology, Cellular Biology and Biochemistry, Brown University, Providence, Rhode Island, United States of America.
Wei LiuInstitute of Plant Protection and Microbiology, Zhejiang Academy of Agricultural Sciences, Hangzhou, China.
Gerwald JoglDepartment of Molecular Biology, Cellular Biology and Biochemistry, Brown University, Providence, Rhode Island, United States of America.
Remo RohsMolecular and Computational Biology Program, Department of Biological Sciences, University of Southern California, Los Angeles, California, United States of America.
Nadia D SinghDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina, United States of America.
Martha L BulykDivision of Genetics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, United States of America.
Michael Y TolstorukovDepartment of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts, United States of America.
Erica LarschanDepartment of Molecular Biology, Cellular Biology and Biochemistry, Brown University, Providence, Rhode Island, United States of America.
Brown University · USMassachusetts General Hospital · USUniversity of Southern California · USBoston University · USBrigham and Women's Hospital · USInstitute of Plant Protection · CNNorth Carolina State University · USNovartis (United States) · US

Funding

Predoctoral Training in the Molecular Biology of AgingT32AG041688 · NIA · BROWN UNIVERSITY · PI NICOLA NERETTI, John M Sedivy · 2012 to 2026
$3.5M
High-Throughput Identification of Tissue/Cell-Type-Specific Cis Regulatory ModuleR01HG005287 · NHGRI · BRIGHAM AND WOMEN'S HOSPITAL · PI BULYK, MARTHA L · 2010 to 2016
$3.4M
Establishing coordinate gene regulation during Drosophila dosage compensationR01GM098461 · NIGMS · BROWN UNIVERSITY · PI LARSCHAN, ERICA NICOLE · 2011 to 2016
$2.1M
Multi-scale modeling of genetic variation in a developmental networkU01GM103804 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI DEPACE, ANGELA H, MARJORAM, PAUL · 2013 to 2016
$2.0M
Genome analysis based on the integration of DNA sequence and shapeR01GM106056 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ROHS, REMO · 2014 to 2017
$1.3M
NHGRI NIH HHS R01 HG005287NIA NIH HHS T32 AG041688NIGMS NIH HHS R01 GM098461NIGMS NIH HHS R01 GM106056NIGMS NIH HHS U01 GM103804
6 · The paper itself

Abstract

Dosage compensation is an essential process that equalizes transcript levels of X-linked genes between sexes by forming a domain of coordinated gene expression. Throughout the evolution of Diptera, many different X-chromosomes acquired the ability to be dosage compensated. Once each newly evolved X-chromosome is targeted for dosage compensation in XY males, its active genes are upregulated two-fold to equalize gene expression with XX females. In Drosophila melanogaster, the CLAMP zinc finger protein links the dosage compensation complex to the X-chromosome. However, the mechanism for X-chromosome identification has remained unknown. Here, we combine biochemical, genomic and evolutionary approaches to reveal that expansion of GA-dinucleotide repeats likely accumulated on the X-chromosome over evolutionary time to increase the density of CLAMP binding sites, thereby driving the evolution of dosage compensation. Overall, we present new insight into how subtle changes in genomic architecture, such as expansions of a simple sequence repeat, promote the evolution of coordinated gene expression.

Indexed as

Dinucleotide RepeatsDosage Compensation, GeneticAmino Acid MotifsAnimalsBinding SitesBiological EvolutionDNADNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsFemaleGene DosageGenes, X-LinkedGenetic LinkageGenome, InsectMaleCLAMP protein, DrosophilaDNADNA-Binding ProteinsDrosophila Proteins

Identifiers

PMID27414415
PMCPMC4945028
OpenAlexW2464987744

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.