Molecular Biology

, Volume 41, Issue 6, pp 886–893

Homology-dependent inactivation of LTR retrotransposons in Aspergillus fumigatus and A. nidulans genomes

Genomics. Transcriptomics. Proteomics

DOI: 10.1134/S0026893307060039

Cite this article as:
Novikova, O.S., Fet, V. & Blinov, A.G. Mol Biol (2007) 41: 886. doi:10.1134/S0026893307060039


The repeat-induced point mutation mechanism (RIP) is the most intriguing among the known mechanisms of homology-dependent gene inactivation (silencing) because of its ability to produce irreversible mutations in repetitive DNA sequences. Discovered for the first time in Neurospora crassa, RIP is characterized by C:G to T:A transitions in duplicated sequences. The mechanisms and range of occurrence of RIP are still poorly understood. Mobile elements, including retrotransposons, are a common target for the processes that lead to homology-dependent silencing because of their ability to propagate themselves. Comparative analysis of LTR retrotransposons was performed throughout the genomes of two ascomycetes, Aspergillus fumigatus and A. nidulans. “De-RIP” retroelements were reconstructed on the basis of several copies. CpG, CpA, and TpG sites, which are potential targets for mutagenesis, were found at a much lower frequency in mobile elements than in structural genes. The dinucleotide targets of the two species are affected by RIP at different frequencies: mutagenesis occurs at both CpG and CpA sites in A. fumigatus and is confined to CpG dinucleotides in A. nidulans. This work provides a theoretical background for planning the experimental investigation of RIP inactivation in aspergilli.

Key words

AspergillusLTR retrotransposonsin silico analysismutagenesisRIP inactivation

Copyright information

© Pleiades Publishing, Inc. 2007

Authors and Affiliations

  1. 1.Institute of Cytology and Genetics, Siberian BranchRussian Academy of SciencesNovosibirskRussia
  2. 2.Marshall UniversityHuntingtonUSA