RNA interference and receptors

@article{,

title = {The plant tRNA 3' processing enzyme has a broad substrate spectrum},

author = {S Schiffer and M Helm and A Théobald-Dietrich and R Giege and A Marchfelder},

url = {http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=11444972},

isbn = {11444972},

year  = {2001},

date = {2001-01-01},

journal = {Biochemistry},

volume = {40},

number = {28},

pages = {8264-8272},

abstract = {To elucidate the minimal substrate for the plant nuclear tRNA 3' processing enzyme, we synthesized a set of tRNA variants, which were subsequently incubated with the nuclear tRNA 3' processing enzyme. Our experiments show that the minimal substrate for the nuclear RNase Z consists of the acceptor stem and T arm. The broad substrate spectrum of the nuclear RNase Z raises the possibility that this enzyme might have additional functions in the nucleus besides tRNA 3' processing. Incubation of tRNA variants with the plant mitochondrial enzyme revealed that the organellar counterpart of the nuclear enzyme has a much narrower substrate spectrum. The mitochondrial RNase Z only tolerates deletion of anticodon and variable arms and only with a drastic reduction in cleavage efficiency, indicating that the mitochondrial activity can only cleave bona fide tRNA substrates efficiently. Both enzymes prefer precursors containing short 3' trailers over extended 3' additional sequences. Determination of cleavage sites showed that the cleavage site is not shifted in any of the tRNA variant precursors.},

note = {0006-2960 

Journal Article},

keywords = {Non-U.S. Gov't, Plant/genetics/*metabolism  RNA, Post-Transcriptional  RNA, Transfer, Tyr/genetics/*metabolism  Substrate Specificity/genetics  Support, Unité ARN},

pubstate = {published},

tppubtype = {article}

}