APOGEE 2:多层机器学习模型用于可解释的线粒体误解变异的预测
Salvatore Daniele Bianco1,2, Luca Parca1,3, Francesco Petrizzelli1
1Bioinformatics Laboratory, Fondazione IRCCS Casa Sollievo della Sofferenza, S. Giovanni Rotondo (FG), Italy.
Nature communications
|August 19, 2023
概括
APOGEE 2 增强了线粒体误解变体的解释,改善了线粒体DNA突变的致病性预测. 这个工具有助于研究人员和临床医生了解遗传疾病的原因.
科学领域:
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
- 生物信息学是一种生物信息学.
背景情况:
- 线粒体功能障碍,通常是由线粒体DNA突变引起的,呈现出不同的临床症状,使变异性致病性解释复杂化.
- 精确评估线粒体遗传变异对于诊断和理解线粒体疾病至关重要.
研究的目的:
- 介绍APOGEE 2,一种用于改善线粒体误解变异的致病性预测的先进组合方法.
- 提高线粒体基因组内的解释变异的准确性和可靠性.
主要方法:
- APOGEE 2采用了以线粒体为中心的整体方法,采用了改进的机器学习模型和精心策划的训练数据集.
- 包括区域性基因组脆弱性评估和氨基酸对蛋白质结构影响的机制分析.
- 根据美国医学遗传学和基因组学学院/分子病理学协会的联合共识建议开发.
主要成果:
- APOGEE 2 展示了用于线粒体误解变异的致病性预测的增强性能指标.
- 提供特定区域的基因组脆弱性见解和对变异效应的详细机制解释.
- 病原性得分和概率预先编译并通过MitImpact数据库访问.
结论:
- APOGEE 2 是解决解释线粒体误解变异的复杂性的一个有价值的工具.
- 促进更准确的遗传诊断和对线粒体疾病的研究.
- 改善了对线粒体疾病中的基因型-表型相关性的理解.
相关概念视频
Animal Mitochondrial Genetics
7.6K
Among all the organelles in an animal cell, only mitochondria have their own independent genomes. Animal mitochondrial DNA is a double-stranded, closed-circular molecule with around 20,000 base pairs. Mitochondrial DNA is unique in that one of its two strands, the heavy, or H, -strand is guanine rich, whereas the complementary strand is cytosine rich and called the light, or L, -strand. Compared to nuclear DNA, mitochondrial DNA has a very low percentage of non-coding regions and is marked by...
7.6K
Improving Translational Accuracy
11.6K
Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
11.6K
Mitochondrial Precursor Proteins
2.6K
Mitochondrial precursors are partially unfolded or loosely folded polypeptide chains. Newly synthesized precursors are inhibited from spontaneously folding into their native conformation by the cytosolic chaperones, heat shock proteins 70 (Hsp70), and mitochondrial import stimulation factors (MSFs). Precursors bound to MSFs are guided to the TOM70-TOM37 receptors, while precursors bound to Hsp70 chaperones are targetted to TOM20-TOM22 receptor complexes.
Most of the mitochondrial...
Most of the mitochondrial...
2.6K
Mitochondrial Protein Sorting
4.4K
Mitochondria are double-membrane organelles of the eukaryotes involved in cellular metabolism, signaling, ATP synthesis, and programmed cell death. Each of these processes requires specific proteins and enzymes that must be correctly sorted to the right mitochondrial subcompartment for the proper functioning of the organelle.
Most of these mitochondrial proteins are encoded by the nucleus and imported to the mitochondria as unfolded or loosely folded precursors. Mitochondrial precursors...
Most of these mitochondrial proteins are encoded by the nucleus and imported to the mitochondria as unfolded or loosely folded precursors. Mitochondrial precursors...
4.4K


