# MitoCommun: a database for decoding mitochondrial communication networks

**Authors:** Xueyan Wu, Danlei Chen, Jitong Feng, Xueying Bu, Shengbo Wu, Jianjun Qiao

PMC · DOI: 10.1186/s12864-026-12549-6 · 2026-01-16

## TL;DR

MitoCommun is a database that organizes and provides access to mitochondrial signaling events across multiple species to better understand how mitochondria communicate.

## Contribution

MitoCommun is a manually curated database of mitochondrial signaling events across five species, offering a comprehensive and accessible platform for studying mitochondrial communication.

## Key findings

- MitoCommun includes 580 signaling events and 233 signaling molecules from five species.
- The database integrates signaling networks across species, biological processes, and organelles.
- It provides detailed annotations and pathways for mitochondrial communication.

## Abstract

Mitochondria are highly dynamic signaling organelles that engage in continuous bidirectional communication with the cytoplasm and participate in biological processes such as cell death, inflammation, and epigenetic modification. Mitochondria receive, process and export various types of signals, ranging from metabolites to non-coding RNAs. Despite their central importance, progress in understanding mitochondrial signaling has been hampered by the fragmented characterization of their communication networks. In this study, we present MitoCommun, a manually curated database comprising 580 mitochondria-derived signaling events from five model species: Homo sapiens, Mus musculus, Rattus norvegicus, Saccharomyces cerevisiae, and Caenorhabditis elegans. Specifically, MitoCommun features 233 well-annotated mitochondrial signaling molecules, defined by either mitochondrial origin or specific organelle localization. These molecular entities have been systematically paired with their receptors and functionally mapped into explicit pathways and interaction networks. Furthermore, we have reconstructed signaling networks across phylogenetically divergent species, functionally distinct biological processes, and inter-organelle communication systems, yielding comprehensive topological maps of mitochondrial signaling cascades. By integrating these resources, MitoCommun establishes a foundational framework for decoding mitochondrial communication and serves as a versatile, user-friendly platform for exploring organelle signaling networks, which is freely accessible at http://mitocommun.qscn.online/.

The online version contains supplementary material available at 10.1186/s12864-026-12549-6.

● Comprehensive data were curated for different mitochondrial communications.

● A user-friendly database was developed for browsing and searching the results.

● Multiple signals and pathways were collected, combining detailed cell stresses.

● Mitochondrial signaling networks were integrated across organisms, organelles and functions.

The online version contains supplementary material available at 10.1186/s12864-026-12549-6.

## Linked entities

- **Species:** Homo sapiens (taxon 9606), Mus musculus (taxon 10090), Rattus norvegicus (taxon 10116), Saccharomyces cerevisiae (taxon 4932), Caenorhabditis elegans (taxon 6239)

## Full-text entities

- **Genes:** TBK1 (TANK binding kinase 1) [NCBI Gene 29110] {aka AIARV, FTDALS4, IIAE8, NAK, T2K}, BAK1 (BCL2 antagonist/killer 1) [NCBI Gene 578] {aka BAK, BAK-LIKE, BCL2L7, CDN1}, P2RY2 (purinergic receptor P2Y2) [NCBI Gene 5029] {aka HP2U, P2RU1, P2U, P2U1, P2UR, P2Y2}, MTLN (mitoregulin) [NCBI Gene 205251] {aka LEMP, LINC00116, MOXI, MPM, NCRNA00116, SMIM37}, RIGI (RNA sensor RIG-I) [NCBI Gene 23586] {aka DDX58, RIG-I, RIG1, RLR-1, SGMRT2}, MDM34 (ERMES complex subunit MDM34) [NCBI Gene 852654] {aka MMM2}, TOM70 (protein channel TOM70) [NCBI Gene 855602] {aka MAS70, MOM72, OMP1}, BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581] {aka BCL2L4}, CHCHD2 (coiled-coil-helix-coiled-coil-helix domain containing 2) [NCBI Gene 51142] {aka C7orf17, MIX17B, MNRR1, NS2TP, PARK22}, STAT1 (signal transducer and activator of transcription 1) [NCBI Gene 6772] {aka CANDF7, IMD31A, IMD31B, IMD31C, ISGF-3, STAT91}, MCA1 (Ca(2+)-dependent cysteine protease MCA1) [NCBI Gene 854372] {aka YCA1}, DNM1 (dynamin-related GTPase DNM1) [NCBI Gene 850686] {aka DRP1}, P2RX7 (purinergic receptor P2X 7) [NCBI Gene 5027] {aka P2X7}, flp-2 (SPREPIRF-amide) [NCBI Gene 181222], CYCS (cytochrome c, somatic) [NCBI Gene 54205] {aka CYC, HCS, THC4}, TFAM (transcription factor A, mitochondrial) [NCBI Gene 7019] {aka MTDPS15, MTTF1, MTTFA, TCF6, TCF6L1, TCF6L2}, FIS1 (Fis1p) [NCBI Gene 854745] {aka MDV2}, TLR9 (toll like receptor 9) [NCBI Gene 54106] {aka CD289}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, RTG3 (Rtg3p) [NCBI Gene 852171], NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, RTG1 (Rtg1p) [NCBI Gene 854087], NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, DIABLO (diablo IAP-binding mitochondrial protein) [NCBI Gene 56616] {aka DFNA64, SMAC}, atfs-1 (Stress activated transcription factor atfs-1) [NCBI Gene 179922], HK2 (hexokinase 2) [NCBI Gene 3099] {aka HKII, HXK2}, egl-20 (Protein Wnt) [NCBI Gene 177821], HSP60 (chaperone ATPase HSP60) [NCBI Gene 850963] {aka CPN60, MIF4, MNA2}, RTG2 (Rtg2p) [NCBI Gene 852640]
- **Diseases:** mitochondrial diseases (MESH:D028361), fibrosis (MESH:D005355), inflammation (MESH:D007249), tumor metastasis (MESH:D009362), inflammatory bowel diseases (MESH:D015212)
- **Chemicals:** TCA (MESH:D014233), carbon (MESH:D002244), choline (MESH:D002794), cortisol (MESH:D006854), adenosine (MESH:D000241), succinate (MESH:D019802), methionine (MESH:D008715), 2-HG (MESH:C019417), Colanic acid (MESH:C004275), S-adenosyl-L-methionine (MESH:D012436), acetyl-CoA (MESH:D000105), Peptides (MESH:D010455), cardiolipin (MESH:D002308), CoQ7 (MESH:C030777), fatty acids (MESH:D005227), amino acids (MESH:D000596), alpha-KG (MESH:D007656), melatonin (MESH:D008550), H2O2 (MESH:D006861), Ca2+ (-), ROS (MESH:D017382), calcium (MESH:D002118), short-chain fatty acids (MESH:D005232), serotonin (MESH:D012701), fumarate (MESH:D005650), spermidine (MESH:D013095), N-(3-oxododecanoyl)-homoserine lactone (MESH:C109860), NAD+ (MESH:D009243), Lipids (MESH:D008055), Steroids (MESH:D013256), ATP (MESH:D000255), AMP (MESH:D000249)
- **Species:** Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Caenorhabditis elegans (species) [taxon 6239], Pseudomonas aeruginosa (species) [taxon 287], Mus musculus (house mouse, species) [taxon 10090], C. elegans [taxon 328850], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Mammalia (mammals, class) [taxon 40674]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12896290/full.md

---
Source: https://tomesphere.com/paper/PMC12896290