Evidence map›Paper›PMID 38352419›Full record

ArticlebioRxiv : the preprint server for biology2024

Evolutionary innovation in conserved regulatory elements across the mammalian tree of life.

Severin Uebbing, Acadia A Kocher, Marybeth Baumgartner, Yu Ji, Suxia Bai, Xiaojun Xing, Timothy Nottoli, James P Noonan

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, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Severin UebbingDepartment of Genetics, Yale School of Medicine, New Haven CT, USA.ORCID 0000-0003-2439-6946
Acadia A KocherDepartment of Genetics, Yale School of Medicine, New Haven CT, USA.ORCID 0009-0009-4034-9876
Marybeth BaumgartnerDepartment of Genetics, Yale School of Medicine, New Haven CT, USA.
Yu JiDepartment of Genetics, Yale School of Medicine, New Haven CT, USA.
Suxia BaiYale Genome Editing Center, Yale School of Medicine, New Haven CT, USA.
Xiaojun XingYale Genome Editing Center, Yale School of Medicine, New Haven CT, USA.
Timothy NottoliYale Genome Editing Center, Yale School of Medicine, New Haven CT, USA.ORCID 0000-0002-2218-5590
James P NoonanDepartment of Genetics, Yale School of Medicine, New Haven CT, USA.ORCID 0000-0001-9632-5835
Yale Cancer Center · USYale University · USThe Netherlands Cancer Institute · NLUtrecht University · NL

Funding

GENETICS AND GENOMICS OF HUMAN DISEASET32HD007149 · NICHD · YALE UNIVERSITY · PI James P Noonan · 1985 to 2026
$8.2M
Modeling uniquely human developmental gene regulatory networks using humanized miceR01HD102030 · NICHD · YALE UNIVERSITY · PI NOONAN, JAMES P · 2020 to 2024
$2.8M
Modeling gene regulatory mechanisms contributing to the evolution of the human cerebral cortexF32HD108935 · NICHD · YALE UNIVERSITY · PI BAUMGARTNER, MARY · 2022 to 2024
$225k
NICHD NIH HHS F32 HD108935NICHD NIH HHS R01 HD102030NICHD NIH HHS T32 HD007149
6 · The paper itself

Abstract

Transcriptional enhancers orchestrate cell type- and time point-specific gene expression programs. Evolution of enhancer sequences can alter target gene expression without causing detrimental misexpression in other contexts. It has long been thought that this modularity allows evolutionary changes in enhancers to escape pleiotropic constraints, which is especially important for evolutionary constrained developmental patterning genes. However, there is still little data supporting this hypothesis. Here we identified signatures of accelerated evolution in conserved enhancer elements across the mammalian phylogeny. We found that pleiotropic genes involved in gene regulatory and developmental processes were enriched for accelerated sequence evolution within their enhancer elements. These genes were associated with an excess number of enhancers compared to other genes, and due to this they exhibit a substantial degree of sequence acceleration over all their enhancers combined. We provide evidence that sequence acceleration is associated with turnover of regulatory function. We studied one acceleration event in depth and found that its sequence evolution led to the emergence of a new enhancer activity domain that may be involved in the evolution of digit reduction in hoofed mammals. Our results provide tangible evidence that enhancer evolution has been a frequent contributor to modifications involving constrained developmental signaling genes in mammals.

Identifiers

PMID38352419
PMCPMC10862883
OpenAlexW4391444925

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.