MitoCarta3.0: an updated mitochondrial proteome now with sub-organelle localization and pathway annotations
By S. Rath, Rohit Sharma, Rahul Gupta, Tslil Ast, Connie Chan, Timothy J. Durham, Russell P. Goodman, Z. Grabarek, Mary E. Haas, Wendy W K Hung and 22 more. Nucleic Acids Res., 2020
1,498 citations recorded by the source corpus.
Abstract The mammalian mitochondrial proteome is under dual genomic control, with 99% of proteins encoded by the nuclear genome and 13 originating from the mitochondrial DNA (mtDNA). We previously developed MitoCarta, a catalogue of over 1000 genes encoding the mammalian mitochondrial proteome. This catalogue was compiled using a Bayesian integration of multiple sequence features and experimental datasets, notably protein mass spectrometry of mitochondria isolated from fourteen murine tissues. Here, we introduce MitoCarta3.0. Beginning with the MitoCarta2.0 inventory, we performed manual review to remove 100 genes and introduce 78 additional genes, arriving at an updated inventory of 1136 human genes. We now include manually curated annotations of sub-mitochondrial localization (matrix, inner membrane, intermembrane space, outer membrane) as well as assignment to 149 hierarchical ‘MitoPathways’ spanning seven broad functional categories relevant to mitochondria. MitoCarta3.0, including sub-mitochondrial localization and MitoPathway annotations, is freely available at http://www.broadinstitute.org/mitocarta and should serve as a continued community resource for mitochondrial biology and medicine.
Subfields: Molecular Biology, Spectroscopy
View Paper: https://www.semanticscholar.org/paper/d5452fc492e68caee39d7c78b971c2b716cdaed8
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
- De-chen Liu
- Hao Li
- Junjie Gao
- Yao Zong
- Peng Liao
- Long Chen
- Minghao Zheng
- Changqing Zhang
Citations in the corpus
- Mitochondrial dysfunction: mechanisms and advances in therapy (2024, background): “202,203 Pathophysiology of mitochondrial dysfunction in common precise molecular mechanisms at play may differ depending on the disease context, common mitochondrial functions and behaviors include compromised bioenergetics, augmented oxidative stress, dysregulated calcium homeostasis, and modi fi…”