Evidence map›Paper›PMID 42313493›Full record

ArticleJCI insight2026

Distal enhancer-insulator module of GDF6 is essential for cochlear formation.

Mohammad Faraz Zafeer, Clemer Abad, Havva Ortabozkoyun, Memoona Ramzan, Guney Bademci, Maria C Robayo, Duygu Duman, Rolen M Quadros, Shengru Guo, Juan I Young and 5 more

Abstract read
In one paragraph

Article in JCI insight, 2026. 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.

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

15 authors.

Mohammad Faraz ZafeerJohn P. Hussman Institute for Human Genomics.
Clemer AbadJohn P. Hussman Institute for Human Genomics.
Havva OrtabozkoyunDr. John T. Macdonald Foundation Department of Human Genetics, and.
Memoona RamzanJohn P. Hussman Institute for Human Genomics.
Guney BademciDr. John T. Macdonald Foundation Department of Human Genetics, and.
Maria C RobayoJohn P. Hussman Institute for Human Genomics.
Duygu DumanDepartment of Audiology, Ankara University Faculty of Health Sciences, Ankara, Turkey.
Rolen M QuadrosMouse Genome Engineering Core Facility, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Shengru GuoJohn P. Hussman Institute for Human Genomics.
Juan I YoungJohn P. Hussman Institute for Human Genomics.
Anthony J GriswoldJohn P. Hussman Institute for Human Genomics.
Channabasavaiah B GurumurthyMouse Genome Engineering Core Facility, University of Nebraska Medical Center, Omaha, Nebraska, USA.
Derek M DykxhoornJohn P. Hussman Institute for Human Genomics.
Katherina WalzJohn P. Hussman Institute for Human Genomics.
Mustafa TekinJohn P. Hussman Institute for Human Genomics.

Funding

Tumor Biology Research ProgramP30CA240139 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Stephen D. Nimer · 2019 to 2026
$24.1M
A Collaborative Search for New Genes for Non-Syndromic DeafnessR01DC009645 · NIDCD · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MUSTAFA TEKIN · 2010 to 2026
$11.8M
Genetic Studies of Inner Ear AnomaliesR01DC012836 · NIDCD · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI TEKIN, MUSTAFA · 2013 to 2017
$3.2M
NCI NIH HHS P30 CA240139NIDCD NIH HHS R01 DC009645NIDCD NIH HHS R01 DC012836
6 · The paper itself

Abstract

Several genes guide inner ear development, and mutations in these genes can cause malformations that result in congenital hearing loss. However, the contribution of noncoding regulatory elements remains largely unclear. This study investigates the function of distal enhancer elements in the transcriptional regulation of GDF6, a gene implicated in cochlear development. Using mouse models with targeted deletions, human inner ear organoids, and CRISPR interference (CRISPRi), we identified a downstream regulatory interval harboring a developmental enhancer required to maintain GDF6 expression during otic epithelial maturation and cochlear morphogenesis. Deletion of this regulatory region or targeting of CRISPRi-based repressors to these regions resulted in decreased GDF6 expression, failure of otic-epithelium development, and prevention of hair cell-like differentiation, reflecting cochlear aplasia observed in patients with corresponding genomic deletions. These findings highlight the contribution of long-range regulatory elements to auditory development and illustrate how their disruption contributes to human deafness.

Indexed as

CochleaEnhancer Elements, GeneticGrowth Differentiation Factor 6AnimalsCell DifferentiationGene Expression Regulation, DevelopmentalHumansMiceGDF6 protein, humanGrowth Differentiation Factor 6DevelopmentGenetic diseasesGeneticsMolecular geneticsStem Cells

Identifiers

PMID42313493
PMCPMC13463603

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Registered trials

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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.