Evidence map›Paper›PMID 20009012›Full record

ArticleGenome research2010

Sex-specific and lineage-specific alternative splicing in primates.

Ran Blekhman, John C Marioni, Paul Zumbo, Matthew Stephens, Yoav Gilad

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Genome research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 177 papers.

0numbers the graph read from it
0cells of the map it votes in
177citing papers in PubMed
–field-weighted citation impact
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

177 citing papers in PubMed, 288 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Expression Divergence in Response to Sex-biased Selection.Molecular biology and evolution · 2025
    Article
  10. Article
  11. Review
  12. Sex Differences in Cochlear Transcriptomes in Horseshoe Bats.Animals : an open access journal from MDPI · 2024
    Article
  13. Quantifying transcriptome diversity: a review.Briefings in functional genomics · 2024
    Review
  14. Article
  15. Review
  16. The impact of chromosomal sex on cardiometabolic health and disease.Trends in endocrinology and metabolism: TEM · 2023
    Review
  17. Article
  18. Article
  19. Article
  20. Article

117 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

Ran BlekhmanDepartment of Human Genetics, University of Chicago, Chicago, Illinois 60637, USA. blekhman@uchicago.edu
John C Marioni
Paul Zumbo
Matthew Stephens
Yoav Gilad
University of Chicago · USUniversity of Southern California · US

Funding

UNIQUELY LABELED AMINO ACIDS FOR PROTEIN NMRS06GM008153 · NIGMS · YORK COLLEGE · PI JOHNSON, LAWRENCE WILLIAM · 1989 to 2008
$13.8M
Genome analysis: statistical methods and applicationsR01HG002585 · NHGRI · UNIVERSITY OF WASHINGTON · PI MATTHEW STEPHENS · 2002 to 2026
$8.4M
Integrating genomics and gene expression analyses to map CVD-associated lociR01HL092206 · NHLBI · UNIVERSITY OF CHICAGO · PI GILAD, YOAV · 2009 to 2021
$7.3M
Natural Selection on Gene Regulation in HumansR01GM077959 · NIGMS · UNIVERSITY OF CHICAGO · PI GILAD, YOAV · 2006 to 2014
$2.9M
Genome analysis: statistical methods and applicationsR56HG002585 · NHGRI · UNIVERSITY OF CHICAGO · PI STEPHENS, MATTHEW · 2023 to 2023
$292k
NHGRI NIH HHS HG002585NHGRI NIH HHS R01 HG002585NHGRI NIH HHS R56 HG002585NHLBI NIH HHS R01 HL092206NIGMS NIH HHS GM077959NIGMS NIH HHS GM08153NIGMS NIH HHS R01 GM077959NIGMS NIH HHS S06 GM008153
6 · The paper itself

Abstract

Comparative studies of gene regulation suggest an important role for natural selection in shaping gene expression patterns within and between species. Most of these studies, however, estimated gene expression levels using microarray probes designed to hybridize to only a small proportion of each gene. Here, we used recently developed RNA sequencing protocols, which sidestep this limitation, to assess intra- and interspecies variation in gene regulatory processes in considerably more detail than was previously possible. Specifically, we used RNA-seq to study transcript levels in humans, chimpanzees, and rhesus macaques, using liver RNA samples from three males and three females from each species. Our approach allowed us to identify a large number of genes whose expression levels likely evolve under natural selection in primates. These include a subset of genes with conserved sexually dimorphic expression patterns across the three species, which we found to be enriched for genes involved in lipid metabolism. Our data also suggest that while alternative splicing is tightly regulated within and between species, sex-specific and lineage-specific changes in the expression of different splice forms are also frequent. Intriguingly, among genes in which a change in exon usage occurred exclusively in the human lineage, we found an enrichment of genes involved in anatomical structure and morphogenesis, raising the possibility that differences in the regulation of alternative splicing have been an important force in human evolution.

Indexed as

Genome, HumanSelection, GeneticAdultAlternative SplicingAnimalsExonsFemaleGene ExpressionGene Expression ProfilingHumansLiverMacaca mulattaMalePan troglodytesRNA, MessengerSex FactorsRNA, Messenger

Identifiers

PMID20009012
PMCPMC2813474
OpenAlexW2122884875

What OpenQuestion holds

Textmetadata
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.