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P1: GRA Final
 Encyclopedia of Physical Science and Technology  EN006H-655  June 29, 2001  21:21







               510                                                                            Gene Expression, Regulation of

































































                      FIGURE 7  A simplistic model for spliceosome assembly. (a) The 5 splice site and the branch site are defined via a
                      direct base pairing between the RNA components of the U1 and U2 snRNPs and the precursor-RNA, respectively.
                      (b) Efficient recruitment of the U snRNPs to the spliceosome is aided by non-snRNP proteins. Thus, SR proteins

                      facilitate U1 snRNP binding to the 5 splice site, whereas U2AF binds to the polypyrimidine tract at the 3 splice
                      site and helps U2 snRNP binding to the branch site. The U4/U6–U5 triple snRNP is recruited to form the mature


                      spliceosome. SR proteins bring the 5 and 3 splice sites in close proximity for the catalytic steps of splicing by making


                      simultaneous contact with splicing factors binding to the 5 and 3 splice sites, respectively (see also Fig. 8).
               U2, U4, U5, and U6), ranging in size from 107 to 210  shared among different U snRNPs, whereas other snRNP
               nucleotides, have been shown to participate in splicing.  proteins are unique to each U snRNP. During spliceosome
               In vivo the snRNAs are found complexed to 6–10 pro-  assembly the ends of the introns are in part identified by
               teins, generating the so-called small nuclear ribonucle-  RNA–RNA base pairing between the precursor-RNA and

               oprotein particles (snRNPs). Some snRNP proteins are  a  U  snRNP  (Fig.  7).  For  example,  the  5 splice  site  is
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