rdf:type |
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lifeskim:mentions |
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pubmed:issue |
12
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pubmed:dateCreated |
1993-8-17
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pubmed:abstractText |
mRNA analogues containing 4-thiouridine residues at selected sites were used to extend our analysis of photo-induced cross-links between mRNA and 16S RNA to cover the entire downstream range between positions +1 and +16 on the mRNA (position +1 is the 5'-base of the P-site codon). No tRNA-dependent cross-links were observed from positions +1, +2, +3 or +5. Position +4 on the mRNA was cross-linked in a tRNA-dependent manner to 16S RNA at a site between nucleotides ca 1402-1415 (most probably to the modified residue 1402), and this was absolutely specific for the +4 position. Similarly, the previously observed cross-link to nucleotide 1052 was absolutely specific for the +6 position. The previously observed cross-links from +7 to nucleotide 1395 and from +11 to 532 were however seen to a lesser extent with certain types of mRNA sequence from neighbouring positions (+6 to +10, and +10 to +13, respectively); no tRNA-dependent cross-links to other sites on 16S RNA were found from these positions, and no cross-linking was seen from positions +14 to +16. In each case the effect of a second cognate tRNA (at the ribosomal A-site) on the level of cross-linking was studied, and the specificity of each cross-link was confirmed by translocation experiments with elongation factor G, using appropriate mRNA analogues.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/8392709-1379176,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8392709-1531520,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8392709-1610836,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8392709-1651232,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8392709-1712292,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8392709-2251116,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8392709-2443708,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8392709-2451022,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8392709-2464693,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8392709-2664777,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8392709-2690012,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8392709-8422963
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cross-Linking Reagents,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Elongation Factor G,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Elongation Factors,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Ribosomal, 16S,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Transfer, Met,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Transfer, Tyr,
http://linkedlifedata.com/resource/pubmed/chemical/Ribonuclease H,
http://linkedlifedata.com/resource/pubmed/chemical/Thiouridine
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0305-1048
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pubmed:author |
|
pubmed:issnType |
Print
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pubmed:day |
25
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pubmed:volume |
21
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2853-9
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:8392709-Base Sequence,
pubmed-meshheading:8392709-Binding Sites,
pubmed-meshheading:8392709-Cross-Linking Reagents,
pubmed-meshheading:8392709-Molecular Sequence Data,
pubmed-meshheading:8392709-Peptide Elongation Factor G,
pubmed-meshheading:8392709-Peptide Elongation Factors,
pubmed-meshheading:8392709-Photochemistry,
pubmed-meshheading:8392709-RNA, Messenger,
pubmed-meshheading:8392709-RNA, Ribosomal, 16S,
pubmed-meshheading:8392709-RNA, Transfer, Met,
pubmed-meshheading:8392709-RNA, Transfer, Tyr,
pubmed-meshheading:8392709-Ribonuclease H,
pubmed-meshheading:8392709-Thiouridine
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pubmed:year |
1993
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pubmed:articleTitle |
Site-directed cross-linking of mRNA analogues to 16S ribosomal RNA; a complete scan of cross-links from all positions between '+1' and '+16' on the mRNA, downstream from the decoding site.
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pubmed:affiliation |
Max-Planck-Institut für Molekulare Genetik, Abteilung Wittmann, Berlin, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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