This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Xu, G L
Right arrow Articles by Bindereif, A
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Xu, G L
Right arrow Articles by Bindereif, A

 Previous Article  |  Next Article 

Mol Cell Biol. 1994 July; 14(7): 4565-4570

trans-spliceosomal U6 RNAs of Crithidia fasciculata and Leptomonas seymouri: deviation from the conserved ACAGAG sequence and potential base pairing with spliced leader RNA.

G L Xu, B Wieland and A Bindereif

Max-Planck-Institut für Molekulare Genetik, Otto-Warburg-Laboratorium, Berlin (Dahlem), Germany.

ABSTRACT

U6 RNA genes from the trypanosomatids Crithidia fasciculata and Leptomonas seymouri have been isolated and sequenced. As in Trypanosoma brucei, the U6 RNA genes in both C. fasciculata and L. seymouri are arranged in close linkage with upstream tRNA genes. The U6 RNA sequences from C. fasciculata and L. seymouri deviate in five and three positions, respectively, from the published T. brucei sequence. Interestingly, both C. fasciculata U6 RNA genes carry a C-->T change at the second position of the ACAGAG hexanucleotide sequence, which is important for splicing function and has been considered phylogenetically invariable. A compensatory base change of the C. fasciculata spliced leader RNA at the highly conserved 5' splice site position +5, G-->A, suggests that an interaction between the 5' splice site region and U6 RNA recently proposed for the yeast cis-splicing system may also occur in trans splicing.


Mol Cell Biol. 1994 July; 14(7): 4565-4570




This article has been cited by other articles:

  • Liang, X.-h., Haritan, A., Uliel, S., Michaeli, S. (2003). trans and cis Splicing in Trypanosomatids: Mechanism, Factors, and Regulation. Eukaryot Cell 2: 830-840 [Full Text]  
  • Li, L., Otake, L. R., Xu, Y.-x., Michaeli, S. (2000). The trans-Spliceosomal U4 RNA from the Monogenetic Trypanosomatid Leptomonas collosoma. CLONING AND IDENTIFICATION OF A TRANSCRIBED tRNA-LIKE ELEMENT THAT CONTROLS ITS EXPRESSION. J. Biol. Chem. 275: 2259-2264 [Abstract] [Full Text]  
  • Schnare, M. N., Gray, M. W. (1999). A Candidate U1 Small Nuclear RNA for Trypanosomatid Protozoa. J. Biol. Chem. 274: 23691-23694 [Abstract] [Full Text]  
  • Sturm, N. R., Campbell, D. A. (1999). The Role of Intron Structures in trans-Splicing and Cap 4 Formation for the Leishmania Spliced Leader RNA. J. Biol. Chem. 274: 19361-19367 [Abstract] [Full Text]  
  • Sturm, N. R., Yu, M. C., Campbell, D. A. (1999). Transcription Termination and 3'-End Processing of the Spliced Leader RNA in Kinetoplastids. Mol. Cell. Biol. 19: 1595-1604 [Abstract] [Full Text]  
  • Tarn, W Y, Steitz, J A (1994). SR proteins can compensate for the loss of U1 snRNP functions in vitro.. Genes Dev. 8: 2704-2717 [Abstract]  
  • Xu, Y.-x., Liu, L., Michaeli, S. (2000). Functional Analyses of Positions across the 5' Splice Site of the Trypanosomatid Spliced Leader RNA. IMPLICATIONS FOR BASE-PAIR INTERACTION WITH U5 AND U6 snRNAs. J. Biol. Chem. 275: 27883-27892 [Abstract] [Full Text]