Literature DB >> 2236077

Enzymatic aminoacylation of an eight-base-pair microhelix with histidine.

C Francklyn1, P Schimmel.   

Abstract

The major determinant for the identity of alanine tRNAs is a single base pair in the acceptor helix that is proximal to the site of amino acid attachment. A 7-base-pair microhelix that recreates the acceptor helix can be charged with alanine. No other examples of charging of small helices with specific amino acids have been reported, to our knowledge. We show here that a 13-base-pair and an 8-base-pair hairpin helix that reconstruct a domain and subdomain, respectively, of histidine tRNAs can be charged with histidine. We also show that transplantation of a base pair that is unique to histidine tRNAs is sufficient to consider histidine acceptance on a domain and subdomain of alanine tRNA. Both alanine and histidine aminoacyl-tRNA synthetases retain specificity for their cognate synthetic substrates. Alanine- and histidine-specific microhelices may resemble a system that arose early in the evolution of charging and coding.

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Year:  1990        PMID: 2236077      PMCID: PMC55016          DOI: 10.1073/pnas.87.21.8655

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  30 in total

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6.  Overproduction and dissection of proteins by the expression-cassette polymerase chain reaction.

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7.  A nucleotide that enhances the charging of RNA minihelix sequence variants with alanine.

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9.  ompT encodes the Escherichia coli outer membrane protease that cleaves T7 RNA polymerase during purification.

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  50 in total

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3.  The acceptor stem in pre-tRNAs determines the cleavage specificity of RNase P.

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4.  The kinetics and specificity of cleavage by RNase P is mainly dependent on the structure of the amino acid acceptor stem.

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5.  Anticodon-independent aminoacylation of an RNA minihelix with valine.

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10.  Effect of G-1 on histidine tRNA microhelix conformation.

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