Abstract

RNA polymerase pauses at different DNA sequences during transcription elongation, and this pausing is associated with distinct conformational state(s) of the elongation complex (EC). Transcription termination by the termination factor Rho, an RNA-dependent molecular motor, requires pausing of the EC in the termination zone of Rho-dependent terminators. We hypothesized that the conformational state(s) of the EC associated with this pausing would influence the action of Rho. Analyses of the pausing behavior of the EC at the termination points of two well known Rho-dependent terminators revealed that Rho prefers actively transcribing complexes for termination. RNA release kinetics from stalled ECs showed that the rate of RNA release by Rho was reduced if the EC was irreversibly backtracked, if its RNA exit channel was modified by an RNA hairpin, or the bridge helix/trigger loop movement in its active site was perturbed. These defects were overcome significantly by enhancing the rate of ATP hydrolysis either by increasing the concentration of ATP or by using a Rho mutant with higher ATPase activity. We propose that the force generated from ATP hydrolysis of Rho is the key factor in dislodging the EC through its molecular motor action, and this process is facilitated when the EC is in a catalytically competent state, undergoing rapid "Brownian ratchet" motion.

Highlights

  • Rho is a homo-hexameric RNA/DNA helicase or translocase capable of dissociating the elongating RNA polymerase from the template DNA by utilizing its RNA-dependent ATPase activity (6 – 8)

  • As pausing of the elongation complex (EC) is associated with the termination points in the termination zone [25, 26], we hypothesized that the conformational state(s) associated with pausing would affect the RNA release process by Rho

  • We propose that the force generated by ATP hydrolysis of Rho is the key factor in dislodging the EC through its molecular motor action, JULY 18, 2008

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Summary

Elongation Complex Preferences of Rho

ATAAACTGCCAGGAATTGGGGATC; located upstream of T7A1 promoter of pRS106 ATAAACTGCCAGGAATTGGGGATC; 5Ј-biotinylated RS58 TTAATACGACTCACTATAGGGAGATCGAGAGGGACACGGGCG. T7 ␾-10 promoter fused to the start site of T7A1 promoter GTCCGGATTGGAGCTTGGGATCC; reverse oligo at BamHI site of pRS106 GCGCGCAAGCTTGCGATCAACAAGGCCATTCATGC, ␭ tR1 forward primer with HindIII site GCGCGCGGATCCCCCCATTCAAGAACAGCAAGCAGC, reverse oligo to generate T7A1-␭ tR1 terminator template TTGTGAGCGCTCACAATTCGGATATATATTAACAATTACCTG; reverse oligo with lac operator sequence, used to generate roadblock downstream of rut sites of T7A1-trp tЈ template GCGCGCCATATGAAAACGCCCCTGGTTACCCG, forward primer with NdeI site to amplify E. coli greB gene GCGCGCCTCGAGCGGTTTCACGTACTCGATAGCATTAAC, reverse primer with XhoI site, without stop codon, to amplify E. coli greB GGAATTGTGAGCGCTCACAATTCCTTCCAGCACACATCGCCTGAAAGACTAG; reverse oligo with lac operator sequence 4 nt downstream of the his pause position, used for PCR amplification with RS83/RS307 on his pause template GAATTGTGAGCGCTCACAATTCTTAGGAAAATTATTGATTTACTG; reverse oligo with lac operator sequence; used to generate roadblock downstream of T7A1 promoter AGCACACATCGCCTGAAAGACTAGTCAGGATGATGGTGATATATTAACAATTACCTG; reverse oligo with his pause sequence; specific for. The process is facilitated when the EC is in a catalytically competent state undergoing rapid “Brownian ratchet” motion

EXPERIMENTAL PROCEDURES
RESULTS
Rate of ATP hydrolysis
Reversible Backtracking of EC
DISCUSSION
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