TY - JOUR
T1 - RNA sequence and secondary structure requiresments for rho-dependent transcription termination
AU - Morgan, William
AU - Bear, David G.
AU - Litchman, Bronwen L.
AU - von Hippel, Peter H.
N1 - Funding Information:
This research was supported In part by USPHS Research Grants GM-15792 and GM-29158 (to PHvH) and GM-32055 (to DGB). WDM was a pre-doctoral trainee of USPHS Training Grant GM-00715 and USPHS Institutional National Research Service Award GM-07759. At Oregon DGB was supported In part by USPHS Postdoctoral Fellowship GM-06676. Part of this work has been presented byWDM to the Graduate School of the University of Oregon in partial fulfillment of the requirements for the Ph.D. degree in Chemistry.
PY - 1985/5/24
Y1 - 1985/5/24
N2 - The interaction of E. coli termination factor rho with the nascent RNA transcript appears to be a central feature of the rho-dependent transcription termination process. Based on in vitro studies of the rho-dependent termination of the transcript initiated at the PR promoter of bacteriophage lambda, and on earlier studies, Morgan, Bear and von Hippel (J. Blol. chem 258, 9565-9574, 1983) proposed a model defining the features of a potential binding site for rho protein on transcripts subject to rho-dependent termination. This model suggested that an effective rho binding site on a nancent RNA transcript ahould be: (i) >70-80 nucleotide residues in length; (ii) essentially unencumbered with stable secondary structure; (iii) relatively sequence non-specific; and (iv) located within a few hundred nucleotide residues upstream of the potential rho-dependent terminus. In this paper we examine the sequences and secondary structures of several transcripts that exhibit rho-dependent termination to test this hypothesis further. Unstructured regions of approximately the expected size and location were found on all the transcripts examined. Though several short specific sequence elements were found to occur in a very similar arrangement on the λPR- and λPL-initiated transcripts of λ phage, no such elements of sequence regularity were found on any of the other rho-dependent transcripts. The results of the sequence comparisons reported here strongly support the generality of the "unstructured binding site" hypothesis for rho-dependent termination.
AB - The interaction of E. coli termination factor rho with the nascent RNA transcript appears to be a central feature of the rho-dependent transcription termination process. Based on in vitro studies of the rho-dependent termination of the transcript initiated at the PR promoter of bacteriophage lambda, and on earlier studies, Morgan, Bear and von Hippel (J. Blol. chem 258, 9565-9574, 1983) proposed a model defining the features of a potential binding site for rho protein on transcripts subject to rho-dependent termination. This model suggested that an effective rho binding site on a nancent RNA transcript ahould be: (i) >70-80 nucleotide residues in length; (ii) essentially unencumbered with stable secondary structure; (iii) relatively sequence non-specific; and (iv) located within a few hundred nucleotide residues upstream of the potential rho-dependent terminus. In this paper we examine the sequences and secondary structures of several transcripts that exhibit rho-dependent termination to test this hypothesis further. Unstructured regions of approximately the expected size and location were found on all the transcripts examined. Though several short specific sequence elements were found to occur in a very similar arrangement on the λPR- and λPL-initiated transcripts of λ phage, no such elements of sequence regularity were found on any of the other rho-dependent transcripts. The results of the sequence comparisons reported here strongly support the generality of the "unstructured binding site" hypothesis for rho-dependent termination.
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U2 - 10.1093/nar/13.10.3739
DO - 10.1093/nar/13.10.3739
M3 - Article
C2 - 2409526
AN - SCOPUS:0022431528
SN - 0305-1048
VL - 13
SP - 3739
EP - 3754
JO - Nucleic acids research
JF - Nucleic acids research
IS - 10
ER -