tRNase Z, which can endonucleolytically remove pre-tRNA 39-end trailers, possesses the signature His domain (HxHxDH; Motif II) of the b-lactamase family of metal-dependent hydrolases. Motif II combines with Motifs III-V on its carboxy side to coordinate two divalent metal ions, constituting the catalytic core. The PxKxRN loop and Motif I on the amino side of Motif II have been suggested to modulate tRNase Z activity, including the anti-determinant effect of CCA in mature tRNA. Ala walks through these two homology blocks reveal residues in which the substitutions unexpectedly reduce catalytic efficiency. While substitutions in Motif II can drastically affect k cat without affecting k M , five-to 15-fold increases in k M are observed with substitutions in several conserved residues in the PxKxRN loop and Motif I. These increases in k M suggest a model for substrate binding. Expressed tRNase Z processes mature tRNA with CCA at the 39 end ;80 times less efficiently than a pre-tRNA possessing natural sequence of the 39-end trailer, due to reduced k cat with no effect on k M , showing the CCA anti-determinant to be a characteristic of this enzyme.
tRNAs are transcribed as precursors and processed in a series of reactions culminating in aminoacylation and translation. Central to tRNA maturation, the 3 end trailer can be endonucleolytically removed by tRNase Z. A flexible arm (FA) extruded from the body of tRNase Z consists of a structured ␣␣ hand that binds the elbow of pre-tRNA. Deleting the FA hand causes an almost 100-fold increase in K m with little change in k cat , establishing its contribution to substrate recognition/binding. Remarkably, a 40-residue Ala scan through the FA hand reveals a conserved leucine at the ascending stalk/hand boundary that causes practically the same increase in K m as the hand deletion, thus nearly eliminating its ability to bind substrate. K m also increases with substitutions in the GP (␣4 -␣5) loop and at other conserved residues in the FA hand predicted to contact substrate based on the co-crystal structure. Substitutions that reduce k cat are clustered in the 10 -11 loop.tRNAs are transcribed as precursors with a 5Ј end leader and 3Ј end trailer. The 5Ј end leader is removed by RNase P. The 3Ј end trailer can be endonucleolytically removed by tRNase Z, which cleaves following the unpaired nucleotide just beyond the 3Ј side of the acceptor stem (the discriminator) leaving a 3Ј-OH ready for CCA addition. In some bacteria and in all archaea and eukaryotes (including their organelles), CCA at the 3Ј end of mature tRNAs is not transcriptionally encoded, and a CCA-adding enzyme is required (1); endonucleolytic processing by tRNase Z is thus a precise and probably essential reaction in the pathway to a mature 3Ј end (2, 3).Interestingly, the 3Ј end CCA is an anti-determinant for tRNase Z that discourages the recycling of mature tRNAs (4 -7), although not in every case (8). Additional functions have been suggested for tRNase Z, including a possible role in human prostate cancer susceptibility (2, 9 -12). In some instances, tRNase Z can recognize and cleave RNAs that are structurally related to pre-tRNAs with 3Ј end extensions (10, 12).tRNase Z is an ancient member of the -lactamase superfamily of metal-dependent hydrolases (2, 13). The signature sequence of this family, the His domain (HXHXDH, Motif II), in conjunction with histidines in Motifs III and V and aspartate in Motif IV, contributes side chains that coordinate two divalent metal ions (14, 15). Additionally, the Glu side chain in HEAT and His in the HST loop (located between Motifs IV and V) apparently function as a pair to facilitate proton transfer at the final stage of reaction (16,17). A Glu-His pair in CPSF-73, the long sought endonuclease responsible for pre-mRNA cleavage and a member of the tRNase Z class of RNA endonucleases (13,16,18), displays the same structure relative to the active site and presumably functions identically in catalysis.Substitutions in Motifs II-V, HEAT, and HST loop residues did not show increases in K m (17,19); thus, these residues apparently contribute to metal ion binding and catalysis without being involved with substrate reco...
© 2 0 0 8 L A N D E S B I O S C I E N C E . D O N O T D I S T R I B U T E .tRNAs are transcribed as precursors with a 5' end leader and a 3' end trailer. In the course of tRNA maturation, RNase P removes the 5' end leader and tRNase Z can endonucleolytically remove the 3' end trailer. A domain remote from the active site of tRNase Z recognizes and binds substrate, principally through contacts with the elbow (D/T loops) of the tRNA. To evaluate possible contacts, processing kinetics was performed using human nuclear encoded pre-tRNA Arg with substitutions in conserved D and T loop nucleotides. Changes in K M observed with some of the substitutions suggest contacts between tRNase Z and substrate tRNA in this region, and changes in tRNA structure provide an additional basis for interpretation of the kinetic effects.
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