PMID:9843401: Difference between revisions

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Revision as of 05:16, 9 January 2010

Huang, L, Ku, J, Pookanjanatavip, M, Gu, X, Wang, D, Greene, PJ and Santi, DV (1998) Identification of two Escherichia coli pseudouridine synthases that show multisite specificity for 23S RNA.Biochemistry 37:15951-7

Abstract Several putative Escherichia coli pseudouridine (Psi) synthases have been identified by iterative searching of genomic databases for ORFs homologous to known Psi synthases [Gustafsson et al. (1996) Nucleic Acids Res. 24, 3756-3762]. Of these, yceC and yfiI were proposed to encode Psi synthases which modify 23S rRNA. In the present work, yceC and yfiI were cloned and overexpressed in E. coli, and the encoded enzymes, YceC and YfiI, were purified to homogeneity. Both proteins converted Urd residues of rRNA to Psi, thus confirming their identities as Psi synthases. However, in in vitro experiments both enzymes extensively modified Urd residues of both 23S rRNA and 16S rRNA. Gene-disruption of yceCresulted in the absence of Psi modification at positions U955, 2504, and 2580 of 23S RNA, thus identifying these sites as in vivo targets for YceC. Likewise, yfiI disruption resulted in the absence of Psi modification at positions U1911, 1917, and possibly 1915 of 23S RNA. Disruption of yceC did not affect the growth under the conditions tested, whereas yfiI-disrupted cells showed a dramatic decrease in growth rate. Since YceC and YfiI hypermodify RNA in vitro, factors in addition to ribonucleotide sequence must contribute to the in vivo specificity of these enzymes.
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Annotations

Gene product Qualifier GO ID GO term name Evidence Code with/from Aspect Notes Status

RluC

GO:0031118

rRNA pseudouridine synthesis

IDA: Inferred from Direct Assay

P

complete

RluC

GO:0009982

pseudouridine synthase activity

IDA: Inferred from Direct Assay

F

His-tagged RluC was purified and incubated with [5‘-32P]UMP-23S rRNA. After digestion with nuclease P1, [5‘-32P]ΨMP was observed by 2d-TLC (Fig. 2).

complete

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