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- W1544147210 abstract "Summary The td group I intron interrupting the thymidylate synthase (TS) gene of phage T4 is a mobile intron that encodes the homing endonuclease I‐TevI. Efficient RNA splicing of the intron is required to restore function of the TS gene, while expression of I‐TevI from within the intron is required to initiate intron mobility. Three distinct layers of regulation temporally limit I‐TevI expression to late in the T4 infective cycle, yet the biological rationale for stringent regulation has not been tested. Here, we deleted key control elements to deregulate I‐TevI expression at early and middle times post T4 infection. Strikingly, we found that deregulation of I‐TevI, or of a catalytically inactive variant, generated a thymidine‐dependent phenotype that is caused by a reduction in td intron splicing. Prematurely terminating I‐TevI translation restores td splicing, full‐length TS synthesis, and rescues the thymidine‐dependent phenotype. We suggest that stringent translational control of I‐TevI evolved to prevent the ribosome from disrupting key structural elements of the td intron that are required for splicing and TS function at early and middle times post T4 infection. Analogous translational regulatory mechanisms in unrelated intron‐open reading frame arrangements may also function to limit deleterious consequences on splicing and host gene function." @default.
- W1544147210 created "2016-06-24" @default.
- W1544147210 creator A5029125718 @default.
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- W1544147210 date "2010-05-19" @default.
- W1544147210 modified "2023-10-16" @default.
- W1544147210 title "Better late than early: delayed translation of intron-encoded endonuclease I-TevI is required for efficient splicing of its host group I intron" @default.
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- W1544147210 doi "https://doi.org/10.1111/j.1365-2958.2010.07216.x" @default.
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