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. 2015 May 18;112(22):6967–6972. doi: 10.1073/pnas.1424909112

Fig. 7.

Fig. 7.

Proposed model of mRNA decapping and recapping in T. brucei. Nascent SL RNA with 5′ triphosphate end is converted to diphosphate by RNA triphosphatase (TbCet1), capped and methylated by a nuclear capping enzyme (TbCgm1), and hypermethylated by a series of cap 4 methyltransferases (collectively indicated as cap 4 MTases). Trans-spliced and polyadenylated cap 4 mRNA can enter the translational pool, whereas unmethylated capped and hypomethylated capped mRNA are subject to either 3′-to-5′ degradation (not shown) or converted into pRNA by a decapping enzyme (TbDcp2). The decapped pRNA can either be degraded by a 5′-3′ exonuclease, or have its 5′ cap restored by TbCe1 and TbCmt1 and then return to the translational pool.