ARN

@article{,

title = {Lead(II) as a probe for investigating RNA structure in vivo},

author = {M Lindell and P Romby and E G Wagner},

url = {http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=11991646},

isbn = {11991646},

year  = {2002},

date = {2002-01-01},

journal = {RNA},

volume = {8},

number = {4},

pages = {534-541},

abstract = {In this communication, we describe a simple and reliable method for RNA structure determination in vivo, using the divalent ion, lead(II), as a structural probe. Lead(II) is known to cleave RNA within single-stranded regions, loops, and bulges, whereas cleavages in double-stranded regions are weaker or absent. Because the ion easily entered bacterial cells, Escherichia coli cultures were treated by addition of 50-100 mM lead(II) acetate for 3-7 min, resulting in partial cleavage of RNA in vivo. Cleavage positions were mapped by reverse transcription analysis of total extracted RNA. Three RNAs were analyzed: tmRNA, CopT (the target of the antisense RNA CopA), and the leader region of the ompF mRNA. All three RNAs had previously been analyzed in vitro, and secondary structure models were available. The results presented here show that lead(II) cleavages in vivo yield detailed structural information for these RNAs, which was in good agreement with the models proposed based on in vitro work. These data illustrate the potential of lead(II) as a sequence-independent RNA structure probe for use in living cells.},

note = {1355-8382 

Journal Article},

keywords = {Base Sequence  Biochemistry/*methods  Comparative Study  Lead/*chemistry/*metabolism  Molecular Sequence Data  Nucleic Acid Conformation  Porins/genetics  RNA/*chemistry/*metabolism  RNA, Messenger/chemistry/metabolism  Support, Non-U.S. Gov't, ROMBY, Unité ARN},

pubstate = {published},

tppubtype = {article}

}