Evidence map›Paper›PMID 37205597›Full record

ArticlebioRxiv : the preprint server for biology2023

CTCF-mediated insulation and chromatin environment modulate

He Fang, Ana R Tronco, Giancarlo Bonora, Truong Nguyen, Jitendra Thakur, Joel B Berletch, Galina N Filippova, Steven Henikoff, Jay Shendure, William S Noble and 2 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed, 6 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

He FangDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, 98195.
Ana R TroncoDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, 98195.
Giancarlo BonoraDepartment of Genome Sciences, University of Washington, Seattle, WA, 98195.
Truong NguyenDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, 98195.
Jitendra ThakurBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, 98109.
Joel B BerletchDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, 98195.
Galina N FilippovaDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, 98195.
Steven HenikoffBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, 98109.
Jay ShendureDepartment of Genome Sciences, University of Washington, Seattle, WA, 98195.
William S NobleDepartment of Genome Sciences, University of Washington, Seattle, WA, 98195.
Christine M DistecheDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, 98195.
Xinxian DengDepartment of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, 98195.
University of Washington · USFred Hutch Cancer Center · US

Funding

University of Washington Center for Nuclear Organization and FunctionU54DK107979 · NIDDK · UNIVERSITY OF WASHINGTON · PI NOBLE, WILLIAM STAFFORD, SHENDURE, JAY ASHOK · 2015 to 2019
$11.8M
UW 4-Dimensional Genomic Organization of Mammalian Embryogenesis CenterUM1HG011586 · NHGRI · UNIVERSITY OF WASHINGTON · PI DISTECHE, CHRISTINE M., NOBLE, WILLIAM STAFFORD · 2020 to 2024
$10.3M
X chromosome regulation and role in aneuploidyR35GM131745 · NIGMS · UNIVERSITY OF WASHINGTON · PI Christine M. Disteche · 2019 to 2026
$4.1M
NHGRI NIH HHS UM1 HG011586NIDDK NIH HHS U54 DK107979NIGMS NIH HHS R35 GM131745
6 · The paper itself

Abstract

Background: The number and escape levels of genes that escape X chromosome inactivation (XCI) in female somatic cells vary among tissues and cell types, potentially contributing to specific sex differences. Here we investigate the role of CTCF, a master chromatin conformation regulator, in regulating escape from XCI. CTCF binding profiles and epigenetic features were systematically examined at constitutive and facultative escape genes using mouse allelic systems to distinguish the inactive X (Xi) and active X (Xa) chromosomes. Results: We found that escape genes are located inside domains flanked by convergent arrays of CTCF binding sites, consistent with the formation of loops. In addition, strong and divergent CTCF binding sites often located at the boundaries between escape genes and adjacent neighbors subject to XCI would help insulate domains. Facultative escapees show clear differences in CTCF binding dependent on their XCI status in specific cell types/tissues. Concordantly, deletion but not inversion of a CTCF binding site at the boundary between the facultative escape gene Conclusion: Our findings indicate that escape from XCI is modulated both by looping and insulation of chromatin via convergent arrays of CTCF binding sites and by compaction and epigenetic features of the surrounding heterochromatin.

Indexed as

Car5bChromatin insulationCTCFEscape from X-chromosome inactivationX-chromosome inactivation

Identifiers

PMID37205597
PMCPMC10187265
OpenAlexW4372319053

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.