Evidence map›Paper›PMID 39364610›Full record

ArticleAmerican journal of medical genetics. Part A2025

Promoter Deletion Leading to Allele Specific Expression in a Genetically Unsolved Case of Primary Ciliary Dyskinesia.

M Makenzie Beaman, Weining Yin, Amanda J Smith, Patrick R Sears, Margaret W Leigh, Thomas W Ferkol, Brendan Kearney, Kenneth N Olivier, Adam J Kimple, Shannon Clarke and 15 more

Abstract readCase Reports
In one paragraph

Article in American journal of medical genetics. Part A, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

25 authors.

M Makenzie BeamanDepartment of Pediatrics, Division of Medical Genetics, Duke University, Durham, North Carolina, USA.
Weining YinMarsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Amanda J SmithMarsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Patrick R SearsMarsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Margaret W LeighMarsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Thomas W FerkolMarsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Brendan KearneyDepartment of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, USA.
Kenneth N OlivierMarsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Adam J KimpleMarsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Shannon ClarkeDepartment of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, USA.
Erin HugginsDepartment of Pediatrics, Division of Medical Genetics, Duke University, Durham, North Carolina, USA.
Erica NadingDepartment of Pediatrics, Division of Medical Genetics, Duke University, Durham, North Carolina, USA.
Seung-Hye JungDepartment of Pediatrics, Division of Medical Genetics, Duke University, Durham, North Carolina, USA.
Apoorva K IyengarUniversity Program in Genetics & Genomics, Duke University, Durham, North Carolina, USA.
Xue ZouDepartment of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, USA.
Hong DangMarsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Alejandro BarreraDepartment of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, USA.
William H MajorosDepartment of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, USA.
Catherine W RehderDepartment of Pathology, Duke University, Durham, North Carolina, USA.
Timothy E ReddyDepartment of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, USA.
Lawrence E OstrowskiMarsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Andrew S AllenDepartment of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, USA.
Michael R KnowlesMarsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Maimoona A ZariwalaMarsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Gregory E CrawfordDepartment of Pediatrics, Division of Medical Genetics, Duke University, Durham, North Carolina, USA.ORCID 0000-0001-6106-2772

Funding

The Impact of COVID-19 on People Living with Rare Diseases and Their FamiliesU2CTR002818 · NCATS · CINCINNATI CHILDRENS HOSP MED CTR · PI Maurizio Macaluso, Michael Wagner · 2019 to 2026
$51.2M
Vector CoreP30DK065988 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Scott H Randell · 2004 to 2026
$26.5M
The Duke FUNCTION Center: Pioneering the comprehensive identification of combinatorial noncoding causes of diseaseRM1HG011123 · NHGRI · DUKE UNIVERSITY · PI GREGORY E CRAWFORD, Raluca Gordan · 2020 to 2026
$21.9M
Longitudinal Characterization of Respiratory Tract Exacerbations and Treatment Responses in Primary Ciliary DyskinesiaU54HL096458 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DELL, SHARON · 2009 to 2023
$20.0M
Yale Center for Mendelian GenomicsUM1HG006504 · NHGRI · YALE UNIVERSITY · PI GERSTEIN, MARK BENDER, GUNEL, MURAT · 2016 to 2020
$14.8M
Pathogenesis of PCD Lung DiseaseR01HL071798 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KNOWLES, MICHAEL R · 2004 to 2021
$7.2M
NHGRI Genome Sequencing Program Coordinating CenterU24HG008956 · NHGRI · RUTGERS, THE STATE UNIV OF N.J. · PI BUYSKE, STEVEN G, MATISE, TARA C. · 2016 to 2020
$4.9M
Functional Studies of Novel Genes Mutated in Primary Ciliary Dyskinesia II: Genotype to PhenotypeR01HL117836 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI OSTROWSKI, LAWRENCE E · 2013 to 2023
$4.4M
University Training Program in Biomolecular and Tissue EngineeringT32GM144291 · NIGMS · DUKE UNIVERSITY · PI Charles A. Gersbach, Tatiana Segura · 2022 to 2026
$2.6M
Identifying Pathogenic Non-Coding Mutations in Rare Mendelian DiseaseR21HG010747 · NHGRI · DUKE UNIVERSITY · PI CRAWFORD, GREGORY E, KISHNANI, PRIYA S. · 2019 to 2020
$433k
Cystic Fibrosis Foundation BOUCHE19R0NCATS NIH HHS U2C TR002818NCATS NIH HHS U2CTR002818NHGRI NIH HHS R21 HG010747NHGRI NIH HHS R21HG010747NHGRI NIH HHS RM1 HG011123NHGRI NIH HHS RM1HG011123NHGRI NIH HHS U24 HG008956NHGRI NIH HHS UM1 HG006504NHGRI NIH HHS UM1HG006504NHLBI NIH HHS R01 HL071798NHLBI NIH HHS R01HL071798NHLBI NIH HHS R01 HL117836NHLBI NIH HHS R01HL117836NHLBI NIH HHS U54 HL096458NHLBI NIH HHS U54HL096458NHLBI NIH HHS X01HL115246-01NIDDK NIH HHS P30 DK065988NIDDK NIH HHS P30-DK065988NIGMS NIH HHS T32 GM144291
6 · The paper itself

Abstract

Variation in the non-coding genome represents an understudied mechanism of disease and it remains challenging to predict if single nucleotide variants, small insertions and deletions, or structural variants in non-coding genomic regions will be detrimental. Our approach using complementary RNA-seq and targeted long-read DNA sequencing can prioritize identification of non-coding variants that lead to disease via alteration of gene splicing or expression. We have identified a patient with primary ciliary dyskinesia with a pathogenic coding variant on one allele of the SPAG1 gene, while the second allele appears normal by whole exome sequencing despite an autosomal recessive inheritance pattern. RNA sequencing revealed reduced SPAG1 transcript levels and exclusive allele specific expression of the known pathogenic allele, suggesting the presence of a non-coding variant on the second allele that impacts transcription. Targeted long-read DNA sequencing identified a heterozygous 3 kilobase deletion of the 5' untranslated region of SPAG1, overlapping the promoter and first non-coding exon. This non-coding deletion was missed by whole exome sequencing and gene-specific deletion/duplication analysis, highlighting the importance of investigating the non-coding genome in patients with "missing" disease-causing variation. This paradigm demonstrates the utility of both RNA and long-read DNA sequencing in identifying pathogenic non-coding variants in patients with unexplained genetic disease.

Indexed as

AllelesPromoter Regions, GeneticCiliary Motility DisordersExome SequencingFemaleHumansKartagener SyndromeMalePedigreeSequence Deletiongene regulationlong‐read sequencingnanoporenon‐coding variantprimary ciliary dyskinesiaRNA sequencing

Identifiers

PMID39364610
PMCPMC11698635

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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.