Evidence map›Paper›PMID 24898194›Full record

ArticleAmerican journal of medical genetics. Part A2014

Donor splice-site mutation in CUL4B is likely cause of X-linked intellectual disability.

Eric R Londin, Jeffrey Adijanto, Nancy Philp, Antonio Novelli, Emilia Vitale, Chiara Perria, Gigliola Serra, Viola Alesi, Saul Surrey, Paolo Fortina

Open access · greenAbstract read
In one paragraph

Article in American journal of medical genetics. Part A, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 28% of its field
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

11 citing papers in PubMed, 15 citations in OpenAlex.

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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

10 authors at 6 institutions in 2 countries.

Eric R LondinComputational Medicine Center, Thomas Jefferson University, Philadelphia, Pennsylvania.
Jeffrey Adijanto
Nancy Philp
Antonio Novelli
Emilia Vitale
Chiara Perria
Gigliola Serra
Viola Alesi
Saul Surrey
Paolo Fortina
Thomas Jefferson University · USUniversity of Sassari · ITCasa Sollievo della Sofferenza · ITFatebenefratelli Hospital · ITIstituto di Cibernetica “Eduardo Caianiello” · ITSapienza University of Rome · IT

Funding

X-Ray Crystallography and Macromolecular CharacterizationP30CA056036 · NCI · THOMAS JEFFERSON UNIVERSITY · PI DANIEL P SILVER · 1995 to 2026
$94.8M
NCI NIH HHS P30 CA056036
6 · The paper itself

Abstract

X-linked intellectual disability is the most common form of cognitive disability in males. Syndromic intellectual disability encompasses cognitive deficits with other medical and behavioral manifestations. Recently, a large family with a novel form of syndromic X-linked intellectual disability was characterized. Eight of 24 members of the family are male and had cognitive dysfunction, short stature, aphasia, skeletal abnormalities, and minor anomalies. To identify the causative gene(s), we performed exome sequencing in three affected boys, both parents, and an unaffected sister. We identified a haplotype consisting of eight variants located in cis within the linkage region that segregated with affected members in the family. Of these variants, two were novel. The first was at the splice-donor site of intron 7 (c.974+1G>T) in the cullin-RING ubiquitin ligase (E3) gene, CUL4B. This variant is predicted to result in failure to splice and remove intron 7 from the primary transcript. The second variant mapped to the 3'-UTR region of the KAISO gene (c.1127T>G). Sanger sequencing validated the variants in these relatives as well as in three affected males and five carriers. The KAISO gene variant was predicted to create a binding site for the microRNAs miR-4999 and miR-4774; however, luciferase expression assays failed to validate increased targeting of these miRNAs to the variant 3'-UTR. This SNP may affect 3'-UTR structure leading to decreased mRNA stability. Our results suggest that the intellectual disability phenotype in this family is caused by aberrant splicing and removal of intron 7 from CUL4B gene primary transcript.

Indexed as

3' Untranslated RegionsBinding SitesCullin ProteinsDNA Mutational AnalysisExomeFemaleGenetic LinkageGenome, HumanHaplotypesHumansMaleMicroRNAsMutationPedigreePhenotypeRNA Splice Sites3' Untranslated RegionsCUL4B protein, humanCullin ProteinsMicroRNAsRNA Splice SitesTranscription FactorsZBTB33 protein, humanexome sequencingintellectual disabilityX-linked

Identifiers

PMID24898194
PMCPMC4404493
OpenAlexW1996160733

What OpenQuestion holds

Textmetadata
LicenceTDM
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.