Literature DB >> 18429816

HMRF1L is a human mitochondrial translation release factor involved in the decoding of the termination codons UAA and UAG.

Yusuke Nozaki1, Noriko Matsunaga, Toshihiro Ishizawa, Takuya Ueda, Nono Takeuchi.   

Abstract

While all essential mammalian mitochondrial factors involved in the initiation and elongation phases of translation have been cloned and well characterized, little is known about the factors involved in the termination process. In the present work, we report the functional analysis of human mitochondrial translation release factors (RF). Here, we show that HMRF1, which had been previously denoted as a human mitochondrial RF, was inactive in in vitro translation system, although it is a mitochondrial protein. Instead, we identified another human mitochondrial RF candidate, HMRF1L, and demonstrated that HMRF1L is indeed a mitochondrial protein that functions specifically as an RF for the decoding of mitochondrial UAA and UAG termination codons in vitro. The identification of the functional mitochondrial RF brings us much closer to a detailed understanding of the translational termination process in mammalian mitochondria as well as to the unraveling of the molecular mechanism of diseases caused by the dys-regulation of translational termination in human mitochondria.

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Year:  2008        PMID: 18429816     DOI: 10.1111/j.1365-2443.2008.01181.x

Source DB:  PubMed          Journal:  Genes Cells        ISSN: 1356-9597            Impact factor:   1.891


  19 in total

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Review 2.  Structural aspects of translation termination on the ribosome.

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Review 8.  Termination of protein synthesis in mammalian mitochondria.

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Journal:  J Biol Chem       Date:  2011-08-26       Impact factor: 5.157

Review 9.  Diversity and Similarity of Termination and Ribosome Rescue in Bacterial, Mitochondrial, and Cytoplasmic Translation.

Authors:  Andrei A Korostelev
Journal:  Biochemistry (Mosc)       Date:  2021-09       Impact factor: 2.487

Review 10.  Mitochondrial Protein Translation: Emerging Roles and Clinical Significance in Disease.

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Journal:  Front Cell Dev Biol       Date:  2021-07-01
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