Regulation of Cell Death by Transfer RNA

被引:20
作者
Hou, Ya-Ming [1 ]
Yang, Xiaolu [2 ,3 ]
机构
[1] Thomas Jefferson Univ, Dept Biochem & Mol Biol, Philadelphia, PA 19107 USA
[2] Univ Penn, Sch Med, Dept Canc Biol, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
关键词
POLYMERASE-III TRANSCRIPTION; CYTOPLASMIC TRANSFER-RNA; SYNONYMOUS CODON CHOICE; CYTOCHROME-C; SACCHAROMYCES-CEREVISIAE; CASPASE-8; ACTIVATION; NUCLEOTIDE EXCHANGE; RESPECTIVE CODONS; ESCHERICHIA-COLI; OXIDATIVE STRESS;
D O I
10.1089/ars.2012.5171
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Significance: Both transfer RNA (tRNA) and cytochrome c are essential molecules for the survival of cells. tRNA decodes mRNA codons into amino-acid-building blocks in protein in all organisms, whereas cytochrome c functions in the electron transport chain that powers ATP synthesis in mitochondrion-containing eukaryotes. Additionally, in vertebrates, cytochrome c that is released from mitochondria is a potent inducer of apoptosis, activating apoptotic proteins (caspases) in the cytoplasm to dismantle cells. A better understanding of both tRNA and cytochrome c is essential for an insight into the regulation of cell life and death. Recent Advances: A recent study showed that the mitochondrion-released cytochrome c can be removed from the cell-death pathway by tRNA molecules. The direct binding of cytochrome c by tRNA provides a mechanism for tRNA to regulate cell death, beyond its role in gene expression. Critical Issues: The nature of the tRNA-cytochrome c binding interaction remains unknown. The questions of how this interaction affects tRNA function, cellular metabolism, and apoptotic sensitivity are unanswered. Future Directions: Investigations into the critical issues raised above will improve the understanding of tRNA in the fundamental processes of cell death and metabolism. Such knowledge will inform therapies in cell death-related diseases.
引用
收藏
页码:583 / 594
页数:12
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