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Machine learning-based prediction reveals kinase MAP4K4 regulates neutrophil differentiation through phosphorylating
Guihua Wang1, Dan Zhang1, Zhifeng He1
1Key Laboratory of Birth Defects and Related Diseases of Women and Children of MOE, Department of Laboratory Medicine, State Key Laboratory of Biotherapy, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China.
Abstract:
Neutrophils, an essential innate immune cell type with a short lifespan, rely on continuous replenishment from bone marrow (BM) precursors. Although it is established that neutrophils are derived from the granulocyte-macrophage progenitor (GMP), the molecular regulators involved in the differentiation process remain poorly understood. Here we developed a random forest-based machine-learning pipeline, NeuRGI (Neutrophil Regulatory Gene Identifier), which utilized Positive-Unlabeled Learning (PU-learning) and neural network-based in silico gene knockout to identify neutrophil regulators. We interrogated features including gene expression dynamics, physiological characteristics, pathological relatedness, and gene conservation for the model training. Our identified pipeline leads to identifying Mitogen-Activated Protein Kinase-4 (MAP4K4) as a novel neutrophil differentiation regulator. The loss of MAP4K4 in hematopoietic stem cells and progenitors in mice induced neutropenia and impeded the differentiation of neutrophils in the bone marrow. By modulating the phosphorylation level of proteins involved in cell apoptosis, such as STAT5A, MAP4K4 delicately regulates cell apoptosis during the process of neutrophil differentiation. Our work presents a novel regulatory mechanism in neutrophil differentiation and provides a robust prediction model that can be applied to other cellular differentiation processes.
Insights
Researchers identified Mitogen-Activated Protein Kinase-4 (MAP4K4) as a key regulator of neutrophil differentiation. Loss of MAP4K4 in mice caused neutropenia, highlighting its crucial role in replenishing neutrophils from bone marrow precursors.
Area of Science:
- Immunology
- Molecular Biology
- Computational Biology
Background:
- Neutrophils are crucial innate immune cells requiring constant replenishment from bone marrow precursors.
- The molecular mechanisms governing neutrophil differentiation from granulocyte-macrophage progenitors (GMPs) are not fully understood.
Purpose of the Study:
- To identify novel molecular regulators of neutrophil differentiation.
- To develop a robust computational model for predicting gene regulators in cellular differentiation.
Main Methods:
- Developed NeuRGI, a machine-learning pipeline using random forest and Positive-Unlabeled Learning (PU-learning).
- Integrated gene expression, physiological, pathological, and conservation data for model training.
- Utilized neural network-based in silico gene knockout to identify regulators.
Main Results:
- Identified Mitogen-Activated Protein Kinase-4 (MAP4K4) as a novel regulator of neutrophil differentiation.
- Mice lacking MAP4K4 in hematopoietic stem cells and progenitors exhibited neutropenia and impaired neutrophil differentiation.
- MAP4K4 regulates neutrophil differentiation by modulating apoptosis-related proteins, including STAT5A.
Conclusions:
- Discovered a novel regulatory mechanism for neutrophil differentiation involving MAP4K4.
- Established NeuRGI as a powerful predictive tool applicable to other cell differentiation processes.
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