Mutational Constraint Analysis Workflow for Overlapping Short Open Reading Frames and Genomic Neighbours
bioRxiv (Cold Spring Harbor Laboratory)
Abstract
Understanding the dark genome is a priority task following the complete sequencing of the human genome. Short open reading frames (sORFs) are a group of largely unexplored elements of the dark genome with the potential for being translated into microproteins. The definitive number of coding and regulatory sORFs is not known, however they could account for up to 1-2% of the human genome. This corresponds to an order of magnitude in the range of canonical coding genes. For a few sORFs a clinical relevance has already been demonstrated, but for the majority of potential sORFs the biological function remains unclear. A major limitation in predicting their disease relevance using large-scale genomic data is the fact that no population-level constraint metrics for genetic variants in sORFs are yet available. To overcome this, we used the recently released gno-mAD 4.0 dataset and analysed the constraint of a consensus set of sORFs and their genomic neighbours. We demonstrate that sORFs are mostly embedded into a moderately constraint genomic context, but within the gencode dataset we identified a subset of highly constrained sORFs comparable to highly constrained canonical genes.
Authors 6
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Universitätsklinikum Aachen · RWTH Aachen University
Affiliation as printed
Institute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University Hospital, Aachen, Germany
scieneers GmbH, Karlsruhe, Germany
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Universitätsklinikum Aachen · RWTH Aachen University
Affiliation as printed
Institute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University Hospital, Aachen, Germany
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Universitätsklinikum Aachen · RWTH Aachen University
Affiliation as printed
Institute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University Hospital, Aachen, Germany
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Universitätsklinikum Aachen · RWTH Aachen University
Affiliation as printed
Institute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University Hospital, Aachen, Germany
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Universitätsklinikum Aachen · RWTH Aachen University
Affiliation as printed
Institute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University Hospital, Aachen, Germany
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Jeremias Krause corresponding Aachen Institute for Human Genetics and Genomic Medicine Medical Faculty
Universitätsklinikum Aachen · RWTH Aachen University
Affiliation as printed
Institute for Human Genetics and Genomic Medicine, Medical Faculty, RWTH Aachen University Hospital, Aachen, Germany
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