Evidence map›Paper›PMID 38559085›Full record

ArticlebioRxiv : the preprint server for biology2024

Functional associations of evolutionarily recent human genes exhibit sensitivity to the 3D genome landscape and disease.

Katherine Fleck, Victor Luria, Nitanta Garag, Amir Karger, Trevor Hunter, Daniel Marten, William Phu, Kee-Myoung Nam, Nenad Sestan, Anne H O'Donnell-Luria and 1 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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, 5 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 4 institutions in 1 country.

Katherine FleckDepartment of Molecular and Cell Biology, University of Connecticut, Storrs, CT 06269, USA.
Victor LuriaDepartment of Neuroscience, Yale School of Medicine, New Haven, CT 06510, USA.
Nitanta GaragDepartment of Molecular and Cell Biology, University of Connecticut, Storrs, CT 06269, USA.
Amir KargerIT-Research Computing, Harvard Medical School, Boston, MA 02115, USA.
Trevor HunterDepartment of Molecular and Cell Biology, University of Connecticut, Storrs, CT 06269, USA.
Daniel MartenDivision of Genetics and Genomics, Boston Children's Hospital, Boston, MA 02115, USA.
William PhuDivision of Genetics and Genomics, Boston Children's Hospital, Boston, MA 02115, USA.
Kee-Myoung NamDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06510, USA.
Nenad SestanDepartment of Neuroscience, Yale School of Medicine, New Haven, CT 06510, USA.
Anne H O'Donnell-LuriaDivision of Genetics and Genomics, Boston Children's Hospital, Boston, MA 02115, USA.ORCID 0000-0001-6418-9592
Jelena ErcegDepartment of Molecular and Cell Biology, University of Connecticut, Storrs, CT 06269, USA.
Broad Institute · USUniversity of Connecticut · USYale University · USHarvard University · US

Funding

Functional Genomics of Human Brain DevelopmentP50MH106934 · NIMH · YALE UNIVERSITY · PI SESTAN, NENAD · 2014 to 2019
$7.9M
1/2 Cell Type and Region-Specific Regulatory Networks in Human Brain Development and DisordersU01MH116488 · NIMH · YALE UNIVERSITY · PI SESTAN, NENAD · 2018 to 2022
$6.5M
Heterogeneity of Forebrain Neural PrecursorsR01NS095654 · NINDS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI HAYDAR, TARIK F, SESTAN, NENAD · 2015 to 2019
$3.4M
1/3 Integrative Genomic Analysis of Human Brain Development and AutismR01MH110926 · NIMH · YALE UNIVERSITY · PI SESTAN, NENAD · 2016 to 2019
$3.2M
Genome Folding and Regulation in Diploid Multicellular OrganismsR35GM146922 · NIGMS · UNIVERSITY OF CONNECTICUT STORRS · PI Jelena Erceg · 2022 to 2026
$2.0M
NIGMS NIH HHS R35 GM146922NIMH NIH HHS P50 MH106934NIMH NIH HHS R01 MH110926NIMH NIH HHS U01 MH116488NINDS NIH HHS R01 NS095654
6 · The paper itself

Abstract

Genome organization is intricately tied to regulating genes and associated cell fate decisions. Here, we examine the positioning and functional significance of human genes, grouped by their lineage restriction level, within the 3D organization of the genome. We reveal that genes of different lineage restriction levels have distinct positioning relationships with both domains and loop anchors, and remarkably consistent relationships with boundaries across cell types. While the functional associations of each group of genes are primarily cell type-specific, associations of conserved genes maintain greater stability across 3D genomic features and disease than recently evolved genes. Furthermore, the expression of these genes across various tissues follows an evolutionary progression, such that RNA levels increase from young lineage restricted genes to ancient genes present in most species. Thus, the distinct relationships of gene evolutionary age, function, and positioning within 3D genomic features contribute to tissue-specific gene regulation in development and disease.

Indexed as

3D genome organizationcell type-specific processesgene evolutiongene function/ontologyhuman accelerated regions (HARs)

Identifiers

PMID38559085
PMCPMC10980080
OpenAlexW4392891802

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.