Literature DB >> 2555264

Group I introns as mobile genetic elements: facts and mechanistic speculations--a review.

B Dujon1.   

Abstract

Group I introns form a structural and functional group of introns with widespread but irregular distribution among very diverse organisms and genetic systems. Evidence is now accumulating that several group I introns are mobile genetic elements with properties similar to those originally described for the omega system of Saccharomyces cerevisiae: mobile group I introns encode sequence-specific double-strand (ds) endoDNases, which recognize and cleave intronless genes to insert a copy of the intron by a ds-break repair mechanism. This mechanism results in: the efficient propagation of group I introns into their cognate sites; their maintenance at the site against spontaneous loss; and, perhaps, their transposition to different sites. The spontaneous loss of group I introns occurs with low frequency by an RNA-mediated mechanism. This mechanism eliminates introns defective for mobility and/or for RNA splicing. Mechanisms of intron acquisition and intron loss must create an equilibrium, which explains the irregular distribution of group I introns in various genetic systems. Furthermore, the observed distribution also predicts that horizontal transfer of intron sequences must occur between unrelated species, using vectors yet to be discovered.

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Year:  1989        PMID: 2555264     DOI: 10.1016/0378-1119(89)90034-6

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  171 in total

1.  I-SceI endonuclease, a new tool for studying DNA double-strand break repair mechanisms in Drosophila.

Authors:  Y Bellaiche; V Mogila; N Perrimon
Journal:  Genetics       Date:  1999-07       Impact factor: 4.562

2.  Isolation of an intron-containing partial sequence of the gene encoding dermatophyte actin (ACT) and detection of a fragment of the transcript by reverse transcription-nested PCR as a means of assessing the viability of dermatophytes in skin scales.

Authors:  C N Okeke; R Tsuboi; M Kawai; M Hiruma; H Ogawa
Journal:  J Clin Microbiol       Date:  2001-01       Impact factor: 5.948

3.  Intronic GIY-YIG endonuclease gene in the mitochondrial genome of Podospora curvicolla: evidence for mobility.

Authors:  C Saguez; G Lecellier; F Koll
Journal:  Nucleic Acids Res       Date:  2000-03-15       Impact factor: 16.971

4.  Purification and characterization of the DNA cleavage and recognition site of I-ScaI mitochondrial group I intron encoded endonuclease produced in Escherichia coli.

Authors:  C Monteilhet; D Dziadkowiec; T Szczepanek; J Lazowska
Journal:  Nucleic Acids Res       Date:  2000-03-01       Impact factor: 16.971

5.  Biochemical characterization of I-CmoeI reveals that this H-N-H homing endonuclease shares functional similarities with H-N-H colicins.

Authors:  M Drouin; P Lucas; C Otis; C Lemieux; M Turmel
Journal:  Nucleic Acids Res       Date:  2000-11-15       Impact factor: 16.971

6.  Recruitment of intron-encoded and co-opted proteins in splicing of the bI3 group I intron RNA.

Authors:  Gurminder S Bassi; Daniela M de Oliveira; Malcolm F White; Kevin M Weeks
Journal:  Proc Natl Acad Sci U S A       Date:  2002-01-02       Impact factor: 11.205

Review 7.  Homing endonucleases: structural and functional insight into the catalysts of intron/intein mobility.

Authors:  B S Chevalier; B L Stoddard
Journal:  Nucleic Acids Res       Date:  2001-09-15       Impact factor: 16.971

8.  Folding of the group I intron ribozyme from the 26S rRNA gene of Candida albicans.

Authors:  Y Zhang; M J Leibowitz
Journal:  Nucleic Acids Res       Date:  2001-06-15       Impact factor: 16.971

9.  FUGOID: functional genomics of organellar introns database.

Authors:  Fei Li; David L Herrin
Journal:  Nucleic Acids Res       Date:  2002-01-01       Impact factor: 16.971

10.  Mobile self-splicing group I introns from the psbA gene of Chlamydomonas reinhardtii: highly efficient homing of an exogenous intron containing its own promoter.

Authors:  O W Odom; S P Holloway; N N Deshpande; J Lee; D L Herrin
Journal:  Mol Cell Biol       Date:  2001-05       Impact factor: 4.272

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