{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Mildenhall KB"],"funding":["NIGMS NIH HHS"],"pagination":["645-55"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC5149407"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["101(4)"],"pubmed_abstract":["Here we demonstrate that the RNase E-based degradosome is required for poly(A) polymerase I (PAP I)-dependent polyadenylation after Rho-independent transcription terminators for both mono- and polycistronic transcripts. Disruption of degradosome assembly in mutants lacking the polynucleotide phosphorylase (PNPase) binding domain led to a significant increase in the level of PNPase synthesized polynucleotide tails in the rpsJ and rpsM polycistronic transcripts and the lpp monocistronic transcript. The polynucleotide tails were mostly located within the coding sequences in the degradosome mutants compared to the wild type control where the majority of the PAP I synthesized poly(A) tails were after the Rho-independent transcription terminators. For the Rho terminated metNIQ operon, the tails "],"journal":["Molecular microbiology"],"pubmed_title":["RNase E-based degradosome modulates polyadenylation of mRNAs after Rho-independent transcription terminators in Escherichia coli."],"pmcid":["PMC5149407"],"funding_grant_id":["R01 GM081554","R01 GM057220","R56 GM057220"],"pubmed_authors":["Chung D","Kushner SR","Maples VF","Wiese N","Mildenhall KB","Mohanty BK"],"additional_accession":[]},"is_claimable":false,"name":"RNase E-based degradosome modulates polyadenylation of mRNAs after Rho-independent transcription terminators in Escherichia coli.","description":"Here we demonstrate that the RNase E-based degradosome is required for poly(A) polymerase I (PAP I)-dependent polyadenylation after Rho-independent transcription terminators for both mono- and polycistronic transcripts. Disruption of degradosome assembly in mutants lacking the polynucleotide phosphorylase (PNPase) binding domain led to a significant increase in the level of PNPase synthesized polynucleotide tails in the rpsJ and rpsM polycistronic transcripts and the lpp monocistronic transcript. The polynucleotide tails were mostly located within the coding sequences in the degradosome mutants compared to the wild type control where the majority of the PAP I synthesized poly(A) tails were after the Rho-independent transcription terminators. For the Rho terminated metNIQ operon, the tails ","dates":{"release":"2016-01-01T00:00:00Z","publication":"2016 Aug","modification":"2025-04-26T14:43:29.381Z","creation":"2019-03-27T02:31:13Z"},"accession":"S-EPMC5149407","cross_references":{"pubmed":["27145979"],"doi":["10.1111/mmi.13413"]}}