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MTERF factors: a multifunction protein family

Authors :
Paola Loguercio Polosa
Maria Nicola Gadaleta
Stefania Deceglie
Palmiro Cantatore
Francesco Bruni
Marina Roberti
Source :
Biomolecular Concepts, Vol 1, Iss 2, Pp 215-224 (2010)
Publication Year :
2010
Publisher :
Walter de Gruyter GmbH, 2010.

Abstract

The MTERF family is a large protein family, identified in metazoans and plants, which consists of four subfamilies, MTERF1, 2, 3 and 4. Mitochondrial localisation was predicted for the vast majority of MTERF family members and demonstrated for the characterised MTERF proteins. The main structural feature of MTERF proteins is the presence of a modular architecture, based on repetitions of a 30-residue module, the mTERF motif, containing leucine zipper-like heptads. The MTERF family includes transcription termination factors: human mTERF, sea urchin mtDBP andDrosophilaDmTTF. In addition to terminating transcription, they are involved in transcription initiation and in the control of mtDNA replication. This multiplicity of functions seems to flank differences in the gene organisation of mitochondrial genomes. MTERF2 and MTERF3 play antithetical roles in controlling mitochondrial transcription: that is, mammalian andDrosophilaMTERF3 act as negative regulators, whereas mammalian MTERF2 functions as a positive regulator. Both proteins contact mtDNA in the promoter region, perhaps establishing interactions, either mutual or with other factors. Regulation of MTERF gene expression in human andDrosophiladepends on nuclear transcription factors NRF-2 and DREF, respectively, and proceeds through pathways which appear to discriminate between factors positively or negatively acting in mitochondrial transcription. In this emerging scenario, it appears that MTERF proteins act to coordinate mitochondrial transcription.

Details

ISSN :
1868503X and 18685021
Volume :
1
Database :
OpenAIRE
Journal :
BioMolecular Concepts
Accession number :
edsair.doi.dedup.....fa9643c1fc53c1d535268e5e3c1b82ee
Full Text :
https://doi.org/10.1515/bmc.2010.015