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https://doi.org/10.1007/s00018-016-2406-8
Title: | H2S biosynthesis and catabolism: new insights from molecular studies | Authors: | Rose P. Moore P.K. Zhu Y.Z. |
Keywords: | 3 mercaptopyruvate sulfurtransferase cystathionine beta synthase cystathionine gamma lyase cysteine dioxygenase hydrogen sulfide immunoglobulin enhancer binding protein reduced nicotinamide adenine dinucleotide (phosphate) dehydrogenase (quinone) sulfide 3-mercaptopyruvate sulphurtransferase cystathionine beta synthase cysteine dioxygenase dioxygenase ETHE1 protein, mouse hydrogen sulfide lyase mitochondrial protein O-succinylhomoserine (thiol)-lyase reduced nicotinamide adenine dinucleotide (phosphate) dehydrogenase (quinone) sulfide quinone reductase sulfurtransferase biosynthesis brain disease catabolism chemical structure detoxification disease association disease model disease predisposition enzyme activity gas analysis human in vivo study nonhuman protein expression Review site directed mutagenesis transgenic animal upregulation animal gene expression regulation gene inactivation genetics metabolism procedures signal transduction Animals Biosynthetic Pathways Carbon-Oxygen Lyases Cystathionine beta-Synthase Cysteine Dioxygenase Dioxygenases Gene Expression Regulation Gene Knockout Techniques Humans Hydrogen Sulfide Mitochondrial Proteins Quinone Reductases Signal Transduction Sulfurtransferases |
Issue Date: | 2017 | Publisher: | Birkhauser Verlag AG | Citation: | Rose P., Moore P.K., Zhu Y.Z. (2017). H2S biosynthesis and catabolism: new insights from molecular studies. Cellular and Molecular Life Sciences 74 (8) : 1391-1412. ScholarBank@NUS Repository. https://doi.org/10.1007/s00018-016-2406-8 | Abstract: | Hydrogen sulfide (H2S) has profound biological effects within living organisms and is now increasingly being considered alongside other gaseous signalling molecules, such as nitric oxide (NO) and carbon monoxide (CO). Conventional use of pharmacological and molecular approaches has spawned a rapidly growing research field that has identified H2S as playing a functional role in cell-signalling and post-translational modifications. Recently, a number of laboratories have reported the use of siRNA methodologies and genetic mouse models to mimic the loss of function of genes involved in the biosynthesis and degradation of H2S within tissues. Studies utilising these systems are revealing new insights into the biology of H2S within the cardiovascular system, inflammatory disease, and in cell signalling. In light of this work, the current review will describe recent advances in H2S research made possible by the use of molecular approaches and genetic mouse models with perturbed capacities to generate or detoxify physiological levels of H2S gas within tissues. © 2016, The Author(s). | Source Title: | Cellular and Molecular Life Sciences | URI: | https://scholarbank.nus.edu.sg/handle/10635/175231 | ISSN: | 1420-682X | DOI: | 10.1007/s00018-016-2406-8 |
Appears in Collections: | Staff Publications Elements |
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