期刊
AMERICAN JOURNAL OF HUMAN GENETICS
卷 108, 期 7, 页码 1283-1300出版社
CELL PRESS
DOI: 10.1016/j.ajhg.2021.05.009
关键词
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资金
- One Brave Idea Initiative
- National Human Genome Research Institute of the National Institutes of Health Center of Excellence in Genomic Science Initiative [HG004233, HG010461]
- Canada Excellence Research Chairs
- Canadian Institutes of Health Research Foundation Grant
- Czech Health Research Council [NV19-01-00307]
- General University Hospital in Prague [RVO-VFN64165]
- Swiss National Science Foundation [310030_192505]
- Swiss National Science Foundation (SNF) [310030_192505] Funding Source: Swiss National Science Foundation (SNF)
Most rare clinical missense variants, including the MTHFR variant impact, cannot be easily classified, as variant effects in MTHFR deficiency depend on environmental factors. The MTHFR atlas scores can differentiate pathogenic from benign variants and correlate with disease onset age in severe MTHFR deficiency. The atlas provides insights on structure-function relationships and the impact of genetic background on missense variations.
Most rare clinical missense variants cannot currently be classified as pathogenic or benign. Deficiency in human 5,10-methylenetetrahydrofolate reductase (MTHFR), the most common inherited disorder of folate metabolism, is caused primarily by rare missense variants. Further complicating variant interpretation, variant impacts often depend on environment. An important example of this phenomenon is the MTHFR variant p.Ala222Val (c.665C>T), which is carried by half of all humans and has a phenotypic impact that depends on dietary folate. Here we describe the results of 98,336 variant functional-impact assays, covering nearly all possible MTHFR amino acid substitutions in four folinate environments, each in the presence and absence of p.Ala222Val. The resulting atlas of MTHFR variant effects reveals many complex dependencies on both folinate and p.Ala222Val. MTHFR atlas scores can distinguish pathogenic from benign variants and, among individuals with severe MTHFR deficiency, correlate with age of disease onset. Providing a powerful tool for understanding structure-function relationships, the atlas suggests a role for a disordered loop in retaining cofactor at the active site and identifies variants that enable escape of inhibition by S-adenosylmethionine. Thus, a model based on eight MTHFR variant effect maps illustrates how shifting landscapes of environment- and genetic-background-dependent missense variation can inform our clinical, structural, and functional understanding of MTHFR deficiency.
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