Evidence map›Paper›PMID 19586922›Full record

ArticleHuman molecular genetics2009

Inactive X chromosome-specific reduction in placental DNA methylation.

Allison M Cotton, Luana Avila, Maria S Penaherrera, Joslynn G Affleck, Wendy P Robinson, Carolyn J Brown

Abstract read
In one paragraph

Article in Human molecular genetics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

48 citing papers in PubMed.

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  19. Association of mitofusin 2 methylation and essential hypertension: a case-control study in a Chinese population.Hypertension research : official journal of the Japanese Society of Hypertension · 2018
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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Allison M CottonDepartment of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.
Luana Avila
Maria S Penaherrera
Joslynn G Affleck
Wendy P Robinson
Carolyn J Brown

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome-wide levels of DNA methylation vary between tissues, and compared with other tissues, the placenta has been reported to demonstrate a global decrease in methylation as well as decreased methylation of X-linked promoters. Methylation is one of many features that differentiate the active and inactive X, and it is well established that CpG island promoters on the inactive X are hypermethylated. We now report a detailed analysis of methylation at different regions across the X in male and female placenta and blood. A significant (P < 0.001) placental hypomethylation of LINE1 elements was observed in both males and females. Relative to blood placental promoter hypomethylation was only observed for X-linked, not autosomal promoters, and was significant for females (P < 0.0001) not males (P = 0.9266). In blood, X-linked CpG island promoters were shown to have moderate female methylation (66% across 70 assays) and low (23%) methylation in males. A similar methylation pattern in blood was observed for approximately 20% of non-island promoters as well as 50% of the intergenic or intragenic CpG islands, the latter is likely due to the presence of unannotated promoters. Both intragenic and intergenic regions showed similarly high methylation levels in male and female blood (68 and 66%) while placental methylation of these regions was lower, particularly in females. Thus placental hypomethylation relative to blood is observed globally at repetitive elements as well as across the X. The decrease in X-linked placental methylation is consistently greater in females than males and implicates an inactive X specific loss of methylation in the placenta.

Indexed as

DNA MethylationX Chromosome InactivationAdolescentAdultChildChild, PreschoolChromosomes, Human, XCpG IslandsFemaleHumansLong Interspersed Nucleotide ElementsMaleMiddle AgedPlacentaPregnancyPromoter Regions, Genetic

Identifiers

PMID19586922
PMCPMC2742397

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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 OpenQuestion graph.