Characterizing and decoding ultraconserved regions uncovers their regulatory significance in human brain development and disorders

Ultraconserved regions (UCRs) represent genomic elements with perfect sequence conservation across humans, rats, and mice. Though evolutionarily significant, most UCRs' functions remain elusive. Here, by leveraging current reference genomes from 34 species spanning diverse taxonomic groups, we refine the annotation, trace the evolutionary origins, and compile an updated catalog of UCRs. The updated UCRs are mostly 200-400 base pairs long, with lower GC content and SNP density but more deleterious mutations. They first emerge in fish, growing more abundant in vertebrates. Guided by genomic context and functional analyses, we classified them into three categories: type I (within protein-coding genes) mainly encodes brain development splicing regulators; type II (within non-coding genes) associates with lncRNAs linked to brain malignancies; type III (intergenic, 46% overlapping enhancer-like elements) regulates brain development genes. Our findings underscore UCRs' critical roles in human brain development and disorders, offering a framework for investigating their biological significance.

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Publication Details

Journal
Communications Biology
Published
2025-11-27
DOI
https://doi.org/10.1038/s42003-025-09115-3
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
0.00

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article

Characterizing and decoding ultraconserved regions uncovers their regulatory significance in human brain development and disorders

Xiangting Wang, Tao Shen, Xuehan Zhang, Meiting Wang et al.
Communications Biology
RNA Research and Splicing
article

Characterizing and decoding ultraconserved regions uncovers their regulatory significance in human brain development and disorders

Xiangting Wang, Tao Shen, Xuehan Zhang, Meiting Wang, Yun Bai
article en

Abstract

Ultraconserved regions (UCRs) represent genomic elements with perfect sequence conservation across humans, rats, and mice. Though evolutionarily significant, most UCRs' functions remain elusive. Here, by leveraging current reference genomes from 34 species spanning diverse taxonomic groups, we refine the annotation, trace the evolutionary origins, and compile an updated catalog of UCRs. The updated UCRs are mostly 200-400 base pairs long, with lower GC content and SNP density but more deleterious mutations. They first emerge in fish, growing more abundant in vertebrates. Guided by genomic context and functional analyses, we classified them into three categories: type I (within protein-coding genes) mainly encodes brain development splicing regulators; type II (within non-coding genes) associates with lncRNAs linked to brain malignancies; type III (intergenic, 46% overlapping enhancer-like elements) regulates brain development genes. Our findings underscore UCRs' critical roles in human brain development and disorders, offering a framework for investigating their biological significance.

Communications BiologyVol. 8(1)
University of Science and Technology of China (CN), Yanshan University (CN), Anhui Normal University (CN)
National Natural Science Foundation of China, University of Science and Technology of China
Openalex Percentile: Top 67%
RNA Research and Splicing
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