TY - JOUR
T1 - Molecular characterization of the 5′ end of the rudimentary gene in Drosophila and analysis of three p element insertions
AU - Zerges, William
AU - Udvardy, Andor
AU - Schedl, Paul
N1 - Funding Information:
We thank D.Bopp, B.Bucher, R.Doreig, B.Kellum, G.Horabin, K.Louis, M.Samuels, E.Schmidt, and B.Suter for helpful comments and discussions. We also thank S.Tsubota for providing the mutant strains. This work was supported by NIH grant GM25976. W.Z. was supported by NIH Predoctoral Training Grant GM07312.
PY - 1992/9/11
Y1 - 1992/9/11
N2 - A detailed analysis of the 5′ end of the rudimentary gene of Drosophila melanogaster is presented. rudimentary transcripts are heterogeneous at their 5′ ends indicating that transcription is initiated at multiple sites within a region of {reversed tilde}50 bp. These transcription initiation sites are within a region that is preferentially susceptible to nuclease cleavage in isolated nuclei. Additional nuclease hypersensitive regions were found within the first exon and the first intron. Within these internal nuclease hypersensitive regions are the insertion sites for previously identified P element transposons which disrupt rudimentary expression. One of these P element insertions, located in the first intron, is removed from the rudimentary transcript with the splicing of this intron. Another P element insertion, within the first exon, is removed from the rudimentary transcript by novel first intron splicing involving a cryptic splice donor site, located 5′ to the insertion, and either the normal acceptor site or a cryptic splice acceptor site within the second exon.
AB - A detailed analysis of the 5′ end of the rudimentary gene of Drosophila melanogaster is presented. rudimentary transcripts are heterogeneous at their 5′ ends indicating that transcription is initiated at multiple sites within a region of {reversed tilde}50 bp. These transcription initiation sites are within a region that is preferentially susceptible to nuclease cleavage in isolated nuclei. Additional nuclease hypersensitive regions were found within the first exon and the first intron. Within these internal nuclease hypersensitive regions are the insertion sites for previously identified P element transposons which disrupt rudimentary expression. One of these P element insertions, located in the first intron, is removed from the rudimentary transcript with the splicing of this intron. Another P element insertion, within the first exon, is removed from the rudimentary transcript by novel first intron splicing involving a cryptic splice donor site, located 5′ to the insertion, and either the normal acceptor site or a cryptic splice acceptor site within the second exon.
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U2 - 10.1093/nar/20.17.4639
DO - 10.1093/nar/20.17.4639
M3 - Article
C2 - 1329025
AN - SCOPUS:0026760749
SN - 0305-1048
VL - 20
SP - 4639
EP - 4647
JO - Nucleic acids research
JF - Nucleic acids research
IS - 17
ER -