Literature DB >> 2789996

Structures of human and rabbit beta-globin precursor messenger RNAs in solution.

J Teare1, P L Wollenzien.   

Abstract

The structures in solution of human and rabbit beta-globin precursor messenger RNAs containing their first intervening sequence have been investigated. This was accomplished by chemical probing experiments to determine sites of potential base pairing, and by cross-linking experiments to determine the sites of long-range interactions. Secondary structures for both molecules were predicted by using this information. Both molecules are arranged into two separate domains. The first domain, consisting of the first exon, contains several long-range interactions between the beginning of the molecule and sites adjacent to the donor splice site and a partially conserved stem/loop structure. The second domain contains part of the intervening sequence and the beginning of the second exon. The secondary structures involved in the second domain are different in the two molecules. These studies indicate a lack of connection between the donor and acceptor splice sites in these two molecules on the level of the secondary structure. Furthermore, given the absence of strongly conserved structures, it is unlikely that there could be any strict requirements for secondary structures that influence splice site usage.

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Year:  1989        PMID: 2789996     DOI: 10.1021/bi00441a012

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  4 in total

1.  Crosslinking of hnRNP proteins to pre-mRNA requires U1 and U2 snRNPs.

Authors:  S H Mayrand; T Pederson
Journal:  Nucleic Acids Res       Date:  1990-06-11       Impact factor: 16.971

2.  The structure of a pre-mRNA molecule in solution determined with a site directed cross-linking reagent.

Authors:  J Teare; P Wollenzien
Journal:  Nucleic Acids Res       Date:  1990-02-25       Impact factor: 16.971

3.  A 62,000 molecular weight spliceosome protein crosslinks to the intron polypyrimidine tract.

Authors:  J Wang; T Pederson
Journal:  Nucleic Acids Res       Date:  1990-10-25       Impact factor: 16.971

4.  The capacity to form H-DNA cannot substitute for GAGA factor binding to a (CT)n*(GA)n regulatory site.

Authors:  Quinn Lu; John M Teare; Howard Granok; Marci J Swede; Jenny Xu; Sarah C R Elgin
Journal:  Nucleic Acids Res       Date:  2003-05-15       Impact factor: 16.971

  4 in total

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