Small Copy Number Neutral Intrachromosomal Translocation of <i>PAX6</i> and Aniridia

Importance Approximately 5% to 10% of individuals with classic aniridia do not receive a molecular diagnosis after clinical testing for variants in PAX6 and its downstream regulatory region. Objective To apply optical genome mapping (OGM) and long-read whole-genome sequencing (lrWGS) to diagnose an individual with unexplained classic aniridia. Design, Setting, and Participants High-quality DNA was extracted from the blood of a 16-year-old male patient with classic aniridia and prior negative clinical test results that included sequencing and copy number analysis of PAX6 exons and downstream regulatory region as well as genomic analysis via short-read whole-genome sequencing (srWGS) and analyzed using OGM and lrWGS. All analyses were performed in a research laboratory in Wisconsin from January 2019 to September 2025. Interventions OGM and lrWGS. Main Outcomes and Measures Identification of a structural variant disrupting PAX6 expression in an individual with classic aniridia, following negative prior testing including srWGS. Results OGM identified a 55-kb deletion on 11p13 encompassing all PAX6 exons and exon 12 of ELP4 , with insertion of this segment into 11q21. lrWGS delineated the exact breakpoints, confirming that the downstream regulatory region, required for normal PAX6 expression, remained at the 11p13 locus. Consequently, the translocated copy of PAX6 at 11q21 is expected to lack expression due to the loss of its essential regulatory elements. Conclusions and Relevance These findings in an individual with classic aniridia harboring an intrachromosomal rearrangement at the PAX6 locus identified by OGM and lrWGS may represent the smallest reported structural variant to separate the PAX6 coding sequence from its downstream regulatory region. This structural variant may have fallen below the detection threshold of srWGS due to its balanced nature and small size, suggesting OGM and lrWGS would be needed for definitive identification.

Authors

Institutions

Publication Details

Journal
JAMA Ophthalmology
Published
2026-05-14
DOI
https://doi.org/10.1001/jamaophthalmol.2026.1389
Primary Topic
Developmental Biology and Gene Regulation
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Small Copy Number Neutral Intrachromosomal Translocation of PAX6 and Aniridia

Elena V. Semina, Linda M. Reis, Jared Tomei, Ulrich Broeckel et al.
JAMA Ophthalmology
Developmental Biology and Gene Regulation
article

Small Copy Number Neutral Intrachromosomal Translocation of PAX6 and Aniridia

Elena V. Semina, Linda M. Reis, Jared Tomei, Ulrich Broeckel, Ryan Gallagher, Joseph Carroll, Andrea Matter
article en

Abstract

Importance Approximately 5% to 10% of individuals with classic aniridia do not receive a molecular diagnosis after clinical testing for variants in PAX6 and its downstream regulatory region. Objective To apply optical genome mapping (OGM) and long-read whole-genome sequencing (lrWGS) to diagnose an individual with unexplained classic aniridia. Design, Setting, and Participants High-quality DNA was extracted from the blood of a 16-year-old male patient with classic aniridia and prior negative clinical test results that included sequencing and copy number analysis of PAX6 exons and downstream regulatory region as well as genomic analysis via short-read whole-genome sequencing (srWGS) and analyzed using OGM and lrWGS. All analyses were performed in a research laboratory in Wisconsin from January 2019 to September 2025. Interventions OGM and lrWGS. Main Outcomes and Measures Identification of a structural variant disrupting PAX6 expression in an individual with classic aniridia, following negative prior testing including srWGS. Results OGM identified a 55-kb deletion on 11p13 encompassing all PAX6 exons and exon 12 of ELP4 , with insertion of this segment into 11q21. lrWGS delineated the exact breakpoints, confirming that the downstream regulatory region, required for normal PAX6 expression, remained at the 11p13 locus. Consequently, the translocated copy of PAX6 at 11q21 is expected to lack expression due to the loss of its essential regulatory elements. Conclusions and Relevance These findings in an individual with classic aniridia harboring an intrachromosomal rearrangement at the PAX6 locus identified by OGM and lrWGS may represent the smallest reported structural variant to separate the PAX6 coding sequence from its downstream regulatory region. This structural variant may have fallen below the detection threshold of srWGS due to its balanced nature and small size, suggesting OGM and lrWGS would be needed for definitive identification.

JAMA Ophthalmology
Children's Hospital of Wisconsin (US), Medical College of Wisconsin (US)
Openalex Percentile: Top 7%
Developmental Biology and Gene Regulation
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.