TY - JOUR
T1 - Unique structure of new serine tRNAs responsible for decoding leucine codon CUG in various Candida species and their putative ancestral tRNA genes
AU - Ueda, T.
AU - Suzuki, T.
AU - Tokogawa, T.
AU - Nishikawa, K.
AU - Watanabe, K.
N1 - Funding Information:
We thank Drs M Homma and K Tanaka (School of Medicine, Nagoya University), for providing us the strain of C albicans. The authors are also grateful to Drs S Osawa (Biohistory Research Hall) and T Nakase (Institute of Physical and Chemical Research, Wako) for valuable discussions. This work was supported by a Grant-in-Aid for Scientific Research on Priority Areas from the Ministry of Education, Science and Culture of Japan, and by a JSPS Fellowships for Japanese Junior Scientists (to TS).
PY - 1994
Y1 - 1994
N2 - In an asporogenic yeast, Candida cylindracea, codon CUG is not translated as leucine but as serine. On the basis of our recent work on the determination of the genetic code using in vitro translation systems coupled with isolation of the corresponding tRNA molecules, it appears that this non-universal genetic code is unitized not only in C cylindracea but also in various Hemiascomycetes. Here we show that in addition to the species already reported, three pathogenic yeast, C guilliermondii, C lusitaniae and C tropicalis, have tRNASerCAG, indicating that this non-universal genetic code (CUG=Ser) also exists in these species. Determination of their primary structures revealed that the uridine conserved at position 33 in usual tRNAs, is replaced by guanosine or cytidine. This suggests that the three-dimensional structures of the anticodon loop of these tRNAs differ from the conventional structure comprising the U turn in this position. Moreover, we succeeded in isolating putative ancestral serine tRNA genesw hose sequences are highly homologous to tRNASerCAG in each case. These tRNA genes all have the anticodon sequence CGA corresponding to the codon UCG, indicating that tRNASerCAG might have emerged from tRNASerCGA during evolutionary change of the assignment of codon CUG.
AB - In an asporogenic yeast, Candida cylindracea, codon CUG is not translated as leucine but as serine. On the basis of our recent work on the determination of the genetic code using in vitro translation systems coupled with isolation of the corresponding tRNA molecules, it appears that this non-universal genetic code is unitized not only in C cylindracea but also in various Hemiascomycetes. Here we show that in addition to the species already reported, three pathogenic yeast, C guilliermondii, C lusitaniae and C tropicalis, have tRNASerCAG, indicating that this non-universal genetic code (CUG=Ser) also exists in these species. Determination of their primary structures revealed that the uridine conserved at position 33 in usual tRNAs, is replaced by guanosine or cytidine. This suggests that the three-dimensional structures of the anticodon loop of these tRNAs differ from the conventional structure comprising the U turn in this position. Moreover, we succeeded in isolating putative ancestral serine tRNA genesw hose sequences are highly homologous to tRNASerCAG in each case. These tRNA genes all have the anticodon sequence CGA corresponding to the codon UCG, indicating that tRNASerCAG might have emerged from tRNASerCGA during evolutionary change of the assignment of codon CUG.
KW - Candida
KW - anticodon
KW - gene structure
KW - non-universal genetic code
KW - tRNA
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U2 - 10.1016/0300-9084(94)90052-3
DO - 10.1016/0300-9084(94)90052-3
M3 - Article
C2 - 7748957
AN - SCOPUS:0028643574
SN - 0300-9084
VL - 76
SP - 1217
EP - 1222
JO - Biochimie
JF - Biochimie
IS - 12
ER -