Evolutionary History of Calcium-sensing Receptors and Mutations

Khái niệm cốt lõi

Evolutionary analysis of CaSR reveals critical residues for receptor activation and pathogenicity.

Tóm tắt

The study delves into the evolutionary history of the Calcium Sensing Receptor (CaSR) subfamily, focusing on identifying functionally equivalent orthologs, predicting residue significance, and computing specificity-determining position (SDP) scores. The exceptional conservation of the CaSR subfamily is highlighted, with high SDP scores playing a crucial role in receptor activation and pathogenicity. Gradient-boosting trees were utilized to differentiate between gain- and loss-of-function mutations responsible for hypocalcemia and hypercalcemia. The importance of these mutations in receptor activation dynamics was investigated, providing valuable insights into calcium homeostasis regulation and associated disorders.

Thống kê

More than 400 germline loss/gain-of-function mutations cause hypercalcaemic disorders.
Specific residues identified on different domains play crucial roles in CaSR activation.
SDP scores indicate higher specificity in CaSR compared to GPRC6A and TAS1Rs.

Trích dẫn

"The exceptional conservation of the CaSR subfamily is highlighted, with high SDP scores being critical in receptor activation and pathogenicity."
"Specific residues clustered in different regions of the receptor are identified as crucial for proper functioning."

Thông tin chi tiết chính được chắt lọc từ

Evolutionary History of Calcium-Sensing Receptors Unveils Hyper/Hypocalcemia-Causing Mutations

by Bircan,A., K... lúc www.biorxiv.org 06-11-2023

https://www.biorxiv.org/content/10.1101/2023.06.11.544489v2

Yêu cầu sâu hơn

How does the identification of activating and inactivating residues impact potential therapeutic strategies targeting CaSR

The identification of activating and inactivating residues in the Calcium Sensing Receptor (CaSR) has significant implications for potential therapeutic strategies targeting this receptor. By understanding which specific residues are critical for receptor activation or deactivation, researchers can develop more targeted and effective drugs to modulate CaSR activity. For example, if certain mutations are known to cause hypercalcemia or hypocalcemia by either over-activating or inhibiting the receptor, pharmaceutical companies can design drugs that specifically target these residues to restore calcium homeostasis.
Furthermore, knowing the key residues involved in CaSR function allows for the development of personalized medicine approaches. By analyzing a patient's genetic profile and identifying any mutations in these critical residues, healthcare providers can tailor treatment plans to address individual variations in CaSR activity. This precision medicine approach could lead to more effective therapies with fewer side effects.
Overall, the identification of activating and inactivating residues provides valuable insights into the molecular mechanisms underlying CaSR-related disorders and opens up new avenues for developing targeted therapeutics aimed at restoring normal calcium levels.

What implications do the findings have for understanding the evolution of other GPCR families

The findings regarding the evolution of Calcium Sensing Receptors (CaSR) shed light on how G Protein-Coupled Receptor (GPCR) families have diversified over time. The evolutionary analysis of CaSR compared to its closely related subfamilies like GPRC6A and taste receptors provides a framework for understanding how different subfamilies within class C GPCRs have evolved unique functions while sharing common structural features.
By studying the conservation patterns and specificity-determining positions across different subfamilies, researchers can gain insights into how protein families evolve through gene duplication events followed by speciation events. This knowledge is not only applicable to understanding the evolution of other GPCR families but also sheds light on broader themes related to protein family evolution across various biological systems.
Understanding how specific amino acid substitutions impact protein function within a family helps elucidate evolutionary constraints that shape functional diversity among related proteins. These insights can be applied beyond GPCRs to study other protein families where sequence conservation plays a crucial role in maintaining structure-function relationships throughout evolution.

How can machine learning approaches like XGBoost be further optimized for predicting mutation types in proteins

Machine learning approaches like XGBoost offer powerful tools for predicting mutation types in proteins; however, there are ways they can be further optimized:

Feature Engineering: Enhancing feature selection by incorporating additional biophysical properties or evolutionary information about amino acids could improve model performance.

Data Augmentation: Increasing training data through techniques like data augmentation or synthetic data generation may help overcome imbalances between classes such as GoF and LoF mutations.

Hyperparameter Tuning: Fine-tuning parameters like learning rate, tree depth, regularization strength, etc., using grid search or random search methods could optimize model performance.

Ensemble Methods: Implementing ensemble methods by combining multiple XGBoost models trained on different subsets of data could enhance predictive accuracy.

Cross-Validation Strategies: Utilizing advanced cross-validation techniques such as stratified K-fold validation ensures robust evaluation metrics without overfitting.

6 .Interpretability Techniques: Incorporating interpretability techniques like SHAP values enables better understanding of feature importance and enhances model explainability.
By implementing these optimization strategies along with continuous refinement based on feedback from experimental results will lead towards more accurate predictions of mutation types in proteins using machine learning algorithms like XGBoost."