| Autor: |
Andrianova EP; Department of Microbiology, The Ohio State University, Columbus, OH 43210.; Translational Data Analytics Institute, The Ohio State University, Columbus, OH 43210., Marmion RA; The Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544., Shvartsman SY; The Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544.; Department of Molecular Biology, Princeton University, Princeton, NJ 08544.; Flatiron Institute, Simons Foundation, New York, NY 10010., Zhulin IB; Department of Microbiology, The Ohio State University, Columbus, OH 43210.; Translational Data Analytics Institute, The Ohio State University, Columbus, OH 43210. |
| Abstrakt: |
Mutations in signal transduction pathways lead to various diseases including cancers. MEK1 kinase, encoded by the human MAP2 K1 gene, is one of the central components of the MAPK pathway and more than a hundred somatic mutations in the MAP2 K1 gene were identified in various tumors. Germline mutations deregulating MEK1 also lead to congenital abnormalities, such as the cardiofaciocutaneous syndrome and arteriovenous malformation. Evaluating variants associated with a disease is a challenge, and computational genomic approaches aid in this process. Establishing evolutionary history of a gene improves computational prediction of disease-causing mutations; however, the evolutionary history of MEK1 is not well understood. Here, by revealing a precise evolutionary history of MEK1, we construct a well-defined dataset of MEK1 metazoan orthologs, which provides sufficient depth to distinguish between conserved and variable amino acid positions. We matched known and predicted disease-causing and benign mutations to evolutionary changes observed in corresponding amino acid positions and found that all known and many suspected disease-causing mutations are evolutionarily intolerable. We selected several variants that cannot be unambiguously assessed by automated prediction tools but that are confidently identified as "damaging" by our approach, for experimental validation in Drosophila . In all cases, evolutionary intolerant variants caused increased mortality and severe defects in fruit fly embryos confirming their damaging nature. We anticipate that our analysis will serve as a blueprint to help evaluate known and novel missense variants in MEK1 and that our approach will contribute to improving automated tools for disease-associated variant interpretation. |
