Evidence map›Paper›PMID 18074017›Full record

ArticlePloS one2007

Monoallelic expression of multiple genes in the CNS.

Jinhui Wang, Zuzana Valo, David Smith, Judith Singer-Sam

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Monoallelic expression in melanoma.Journal of translational medicine · 2019
    Article
  3. Article
  4. Frequent monoallelic or skewed expression for developmental genes in CNS-derived cells and evidence for balancing selection.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
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  7. Review
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  12. Article
  13. Epigenetics of haematopoietic cell development.Nature reviews. Immunology · 2011
    Review
  14. Article
  15. Review
  16. Article
  17. 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

4 authors at 1 institution in 1 country.

Jinhui WangDivision of Biology, Beckman Research Institute, City of Hope National Medical Center, Duarte, California, United States of America.
Zuzana Valo
David Smith
Judith Singer-Sam
City Of Hope National Medical Center · US

Funding

Monoallelic Expression and Inheritance of CNS DisordersR21MH073754 · NIMH · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI SINGER-SAM, JUDITH · 2006 to 2006
$211k
NIMH NIH HHS R21 MH073754
6 · The paper itself

Abstract

The inheritance pattern of a number of major genetic disorders suggests the possible involvement of genes that are expressed from one allele and silent on the other, but such genes are difficult to detect. Since DNA methylation in regulatory regions is often a mark of gene silencing, we modified existing microarray-based assays to detect both methylated and unmethylated DNA sequences in the same sample, a variation we term the MAUD assay. We probed a 65 Mb region of mouse Chr 7 for gene-associated sequences that show two distinct DNA methylation patterns in the mouse CNS. Selected genes were then tested for allele-specific expression in clonal neural stem cell lines derived from reciprocal F(1) (C57BL/6xJF1) hybrid mice. In addition, using a separate approach, we directly analyzed allele-specific expression of a group of genes interspersed within clusters of OlfR genes, since the latter are subject to allelic exclusion. Altogether, of the 500 known genes in the chromosomal region surveyed, five show monoallelic expression, four identified by the MAUD assay (Agc1, p (pink-eyed dilution), P4ha3 and Thrsp), and one by its proximity to OlfR genes (Trim12). Thrsp (thyroid hormone responsive SPOT14 homolog) is expressed in hippocampus, but the human protein homolog, S14, has also been implicated in aggressive breast cancer. Monoallelic expression of the five genes is not coordinated at a chromosome-wide level, but rather regulated at individual loci. Taken together, our results suggest that at least 1% of previously untested genes are subject to allelic exclusion, and demonstrate a dual approach to expedite their identification.

Indexed as

AllelesGene ExpressionAnimalsCentral Nervous SystemHumansMaleMiceMice, Inbred C57BLOligonucleotide Array Sequence Analysis

Identifiers

PMID18074017
PMCPMC2100171
OpenAlexW2016459834

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.