Identification of Clonal Hematopoiesis Driver Mutations through In Silico Saturation Mutagenesis.
Santiago DemajoJoan Enric Ramis-ZaldivarFerran MuinosMiguel L GrauMaria AndrianovaNúria López-BigasNuria Lopez-BigasPublished in: Cancer discovery (2024)
Clonal hematopoiesis (CH) is a phenomenon of clonal expansion of hematopoietic stem cells driven by somatic mutations affecting certain genes. Recently, CH has been linked to the development of hematologic malignancies, cardiovascular diseases, and other conditions. Although the most frequently mutated CH driver genes have been identified, a systematic landscape of the mutations capable of initiating this phenomenon is still lacking. Here, we trained machine-learning models for 12 of the most recurrent CH genes to identify their driver mutations. These models outperform expert-curated rules based on prior knowledge of the function of these genes. Moreover, their application to identify CH driver mutations across almost half a million donors of the UK Biobank reproduces known associations between CH driver mutations and age, and the prevalence of several diseases and conditions. We thus propose that these models support the accurate identification of CH across healthy individuals.
Keyphrases
- room temperature
- bioinformatics analysis
- machine learning
- genome wide
- cardiovascular disease
- healthcare
- metabolic syndrome
- genome wide identification
- induced apoptosis
- crispr cas
- gene expression
- high resolution
- ionic liquid
- oxidative stress
- dna methylation
- mass spectrometry
- signaling pathway
- coronary artery disease
- clinical practice
- molecular docking
- cell proliferation
- transcription factor
- cell death
- kidney transplantation
- cardiovascular risk factors
- copy number