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- W3090421102 abstract "Abstract As an essential component of the translation machinery, aminoacyl-tRNA synthetases (aaRSs) are indispensable for cell viability. In complex multicellular organisms, this fundamental importance of aaRSs is further expanded by their broad regulatory functions, and reflected by their extensive human disease connections. This chapter focuses on the disease connection of the group of aaRSs supporting protein synthesis in the cytoplasm, including GlyRS and LysRS that are also used for mitochondrial translation. To date, three major disease types have been linked directly to cytoplasmic aaRSs: first, an autoimmune antisynthetase syndrome (ASS) characterized by the presence of autoantibodies targeting one of eight different aaRSs; second, a peripheral neuropathy, Charcot-Marie-Tooth disease (CMT) caused by dominant, mono-allelic mutations in six different aaRSs; and third, severe multi-organ disorders, often accompanied with developmental delays, caused by recessive, bi-allelic mutations in almost all cytoplasmic aaRSs. This chapter will cover broadly each of these types, with a lesser focus on CMT. An interesting feature of cytoplasmic aaRSs in complex organisms is the formation of a multi-synthetase complex (MSC), containing nine aaRSs and three non-enzymatic scaffold proteins. We note a general trend that MSC components are more likely to be involved in recessive diseases, whereas the freestanding aaRSs are predominantly linked to the dominant CMT disease and the autoimmune ASS. GlyRS and LysRS appear to be more susceptive to mutational impact, possibly due to their dual use for cytosolic and mitochondrial protein synthesis. Nevertheless, non-enzymatic functions of aaRSs are also linked to diseases as suggested by studies on ASS and CMT." @default.
- W3090421102 created "2020-10-08" @default.
- W3090421102 creator A5025528517 @default.
- W3090421102 creator A5085148550 @default.
- W3090421102 creator A5089840701 @default.
- W3090421102 date "2020-01-01" @default.
- W3090421102 modified "2023-10-17" @default.
- W3090421102 title "Human diseases linked to cytoplasmic aminoacyl-tRNA synthetases" @default.
- W3090421102 cites W1219892868 @default.
- W3090421102 cites W1495970414 @default.
- W3090421102 cites W1576843479 @default.
- W3090421102 cites W1590288764 @default.
- W3090421102 cites W1750588665 @default.
- W3090421102 cites W1793398124 @default.
- W3090421102 cites W1840470014 @default.
- W3090421102 cites W1922768394 @default.
- W3090421102 cites W1967509044 @default.
- W3090421102 cites W1968296590 @default.
- W3090421102 cites W1968980213 @default.
- W3090421102 cites W1971734001 @default.
- W3090421102 cites W1972326289 @default.
- W3090421102 cites W1974011102 @default.
- W3090421102 cites W1974946256 @default.
- W3090421102 cites W1978368107 @default.
- W3090421102 cites W1979428706 @default.
- W3090421102 cites W1981529363 @default.
- W3090421102 cites W1982347103 @default.
- W3090421102 cites W1987213193 @default.
- W3090421102 cites W1987353768 @default.
- W3090421102 cites W1988294705 @default.
- W3090421102 cites W1989971152 @default.
- W3090421102 cites W1994940875 @default.
- W3090421102 cites W2000040082 @default.
- W3090421102 cites W2001220125 @default.
- W3090421102 cites W2004009723 @default.
- W3090421102 cites W2004089161 @default.
- W3090421102 cites W2006873318 @default.
- W3090421102 cites W2016198366 @default.
- W3090421102 cites W2016658685 @default.
- W3090421102 cites W2024920387 @default.
- W3090421102 cites W2025591541 @default.
- W3090421102 cites W2027453551 @default.
- W3090421102 cites W2028528516 @default.
- W3090421102 cites W2028556406 @default.
- W3090421102 cites W2032003226 @default.
- W3090421102 cites W2037555428 @default.
- W3090421102 cites W2038459981 @default.
- W3090421102 cites W2039039501 @default.
- W3090421102 cites W2039126449 @default.
- W3090421102 cites W2040223620 @default.
- W3090421102 cites W2041273068 @default.
- W3090421102 cites W2045337148 @default.
- W3090421102 cites W2045497860 @default.
- W3090421102 cites W2045930677 @default.
- W3090421102 cites W2048446407 @default.
- W3090421102 cites W2048716562 @default.
- W3090421102 cites W2050299992 @default.
- W3090421102 cites W2051103305 @default.
- W3090421102 cites W2052676309 @default.
- W3090421102 cites W2057122890 @default.
- W3090421102 cites W2065744472 @default.
- W3090421102 cites W2069599749 @default.
- W3090421102 cites W2073240987 @default.
- W3090421102 cites W2075072186 @default.
- W3090421102 cites W2079298713 @default.
- W3090421102 cites W2085382985 @default.
- W3090421102 cites W2087178593 @default.
- W3090421102 cites W2087887605 @default.
- W3090421102 cites W2094671725 @default.
- W3090421102 cites W2095250665 @default.
- W3090421102 cites W2098063632 @default.
- W3090421102 cites W2098918246 @default.
- W3090421102 cites W2100534662 @default.
- W3090421102 cites W2102270499 @default.
- W3090421102 cites W2103590517 @default.
- W3090421102 cites W2106440646 @default.
- W3090421102 cites W2108093337 @default.
- W3090421102 cites W2112960652 @default.
- W3090421102 cites W2122161608 @default.
- W3090421102 cites W2124501518 @default.
- W3090421102 cites W2126418361 @default.
- W3090421102 cites W2127075206 @default.
- W3090421102 cites W2128151490 @default.
- W3090421102 cites W2128834219 @default.
- W3090421102 cites W2130147500 @default.
- W3090421102 cites W2130940389 @default.
- W3090421102 cites W2131102106 @default.
- W3090421102 cites W2133210342 @default.
- W3090421102 cites W2135791473 @default.
- W3090421102 cites W2136990296 @default.
- W3090421102 cites W2137748756 @default.
- W3090421102 cites W2137816646 @default.
- W3090421102 cites W2139544990 @default.
- W3090421102 cites W2141416163 @default.
- W3090421102 cites W2141699260 @default.
- W3090421102 cites W2143372911 @default.
- W3090421102 cites W2146747110 @default.
- W3090421102 cites W2148869194 @default.