Evidence map›Paper›PMID 26848384›Full record

ArticleBiology of sex differences2016

The phenotypic impact of the male-specific region of chromosome-Y in inbred mating: the role of genetic variants and gene duplications in multiple inbred rat strains.

Jeremy W Prokop, Shirng-Wern Tsaih, Allison B Faber, Shannon Boehme, Adam C Underwood, Samuel Troyer, Lauren Playl, Amy Milsted, Monte E Turner, Daniel Ely and 5 more

Open access · goldAbstract read
In one paragraph

Article in Biology of sex differences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
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  8. Review
  9. Article
  10. Article
  11. Review
  12. The Y chromosome: a blueprint for men's health?European journal of human genetics : EJHG · 2017
    Review
  13. Genetic variation in chromosome Y regulates susceptibility to influenza A virus infection.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  14. Article
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 5 institutions in 2 countries.

Jeremy W ProkopHudsonAlpha Institute for Biotechnology, 601 Genome Way, Huntsville, AL 35806 USA ; Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, WI 53226 USA ; Department of Physiology, Medical College of Wisconsin, Milwaukee, WI 53226 USA.
Shirng-Wern TsaihHuman and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, WI 53226 USA.
Allison B FaberHuman and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, WI 53226 USA ; Department of Physiology, Medical College of Wisconsin, Milwaukee, WI 53226 USA.
Shannon BoehmeDepartment of Biology, The University of Akron, Akron, OH 44325 USA.
Adam C UnderwoodDepartment of Mathematics and Science, Walsh University, North Canton, OH 44720 USA.
Samuel TroyerDepartment of Biology, The University of Akron, Akron, OH 44325 USA.
Lauren PlaylDepartment of Biology, The University of Akron, Akron, OH 44325 USA.
Amy MilstedDepartment of Biology, The University of Akron, Akron, OH 44325 USA.
Monte E TurnerDepartment of Biology, The University of Akron, Akron, OH 44325 USA.
Daniel ElyDepartment of Biology, The University of Akron, Akron, OH 44325 USA.
Almir S MartinsNúcleo de Fisiologia Geral e Genômica Funcional-ICB-Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, Minas Gerais Brazil.
Marek TutajHuman and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, WI 53226 USA.
Jozef LazarHudsonAlpha Institute for Biotechnology, 601 Genome Way, Huntsville, AL 35806 USA ; Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, WI 53226 USA ; Department of Physiology, Medical College of Wisconsin, Milwaukee, WI 53226 USA.
Melinda R DwinellHuman and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, WI 53226 USA ; Department of Physiology, Medical College of Wisconsin, Milwaukee, WI 53226 USA.
Howard J JacobHudsonAlpha Institute for Biotechnology, 601 Genome Way, Huntsville, AL 35806 USA ; Human and Molecular Genetics Center, Medical College of Wisconsin, Milwaukee, WI 53226 USA ; Department of Physiology, Medical College of Wisconsin, Milwaukee, WI 53226 USA.
Medical College of Wisconsin · USUniversity of Akron · USHudsonAlpha Institute for Biotechnology · USUniversidade Federal de Minas Gerais · BRWalsh University · US

Funding

Physiological Genomics of Hypertensive Renal DiseaseR01HL069321 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI LAZAR, JOZEF · 2001 to 2017
$5.6M
Tyrosine Hydroxylase Sry and HypertensionR01HL071579 · NHLBI · UNIVERSITY OF AKRON · PI ELY, DANIEL L · 2005 to 2009
$1.8M
Using a Sequence-to-Structure-to-Function Approach to Functionally Characterize Protein Coding Missense Mutations in the Human and Rat GenomesK01ES025435 · NIEHS · MICHIGAN STATE UNIVERSITY · PI PROKOP, JEREMY WILLIAM · 2014 to 2018
$489k
NHLBI NIH HHS R01 HL069321NHLBI NIH HHS R01 HL071579NIEHS NIH HHS K01 ES025435
6 · The paper itself

Abstract

backgoundThe male-specific region of chromosome-Y (MSY) contributes to phenotypes outside of testis development and has a high rate of evolution between mammalian species. With a lack of genomic crossover, MSY is one of the few genomic areas under similar variation and evolutionary selection in inbred and outbred animal populations, allowing for an assessment of evolutionary mechanisms to translate between the populations.

methodsUsing next-generation sequencing, MSY consomic strains, molecular characterization, and large-scale phenotyping, we present here regions of MSY that contribute to inbred strain phenotypes.

resultsWe have shown that (1) MSY of rat has nine autosomal gene transposition events with strain-specific selection; (2) sequence variants in MSY occur with a 1.98-fold higher number of variants than other chromosomes in seven sequenced rat strains; (3) Sry, the most studied MSY gene, has undergone extensive gene duplications, driving ubiquitous expression not seen in human or mouse; (4) the expression profile of Sry in the rat is driven by the insertion of the Sry2 copy into an intron of the ubiquitously expressed Kdm5d gene in antisense orientation, but due to several loss of function mutations in the Sry2 protein, nuclear localization and transcriptional control are decreased; (5) expression of Sry copies other than Sry2 in the rat overlaps with the expression profile for human SRY; (6) gene duplications and sequence variants (P76T) of Sry can be selected for phenotypes such as high blood pressure and androgen receptor signaling within inbred mating; and most importantly, (7) per chromosome size, MSY contributes to higher strain-specific phenotypic variation relative to all other chromosomes, with 53 phenotypes showing both a male to female and consomic cross significance.

conclusionThe data presented supports a high probability of MSY genetic variation altering a broad range of inbred rat phenotypes.

Indexed as

Gene duplicationsInbred matingMed14yMSYPhenotypic variationRattus norvegicusSryUbe2q2y

Identifiers

PMID26848384
PMCPMC4740989
OpenAlexW2255467143

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

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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 Socratic graph.