Extensive, nonrandom diversity of excision footprints generated by Ds-like transposon Ascot-1 suggests new parallels with V(D)J recombination

• Published in: Molecular and cellular biology Vol. 18; no. 7; pp. 4337 - 4346
• Main Authors: Colot, V, Haedens, V, Rossignol, J L
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 01-07-1998
• Subjects: Ascomycota - genetics; Base Sequence; Color; DNA; DNA Dynamics and Chromosome Structure; DNA Footprinting; DNA Transposable Elements; Genetic Variation; Genome, Fungal; Immunoglobulin delta-Chains - genetics; Immunoglobulin Joining Region - genetics; Immunoglobulin Variable Region - genetics; Molecular Sequence Data; Mutagenesis, Insertional; Phenotype; Recombination, Genetic; Spores, Fungal
• ISSN: 0270-7306; 1098-5549; 1098-5549
• DOI: 10.1128/MCB.18.7.4337

Upon insertion, transposable elements can disrupt or alter gene function in various ways. Transposons moving through a cut-and-paste mechanism are in addition often mutagenic when excising because repair of the empty site seldom restores the original sequence. The characterization of numerous excision events in many eukaryotes indicates that transposon excision from a given site can generate a high degree of DNA sequence and phenotypic variation. Whether such variation is generated randomly remains largely to be determined. To this end, we have exploited a well-characterized system of genetic instability in the fungus Ascobolus immersus to perform an extensive study of excision events. We show that this system, which produces many phenotypically and genetically distinct derivatives, results from the excision of a novel Ds-like transposon, Ascot-1, from the spore color gene b2. A unique set of 48 molecularly distinct excision products were readily identified from a representative sample of excision derivatives. Products varied in their frequency of occurrence over 4 orders of magnitude, yet most showed small palindromic nucleotide additions. Based on these and other observations, compelling evidence was obtained for intermediate hairpin formation during the excision reaction and for strong biases in the subsequent processing steps at the empty site. Factors likely to be involved in these biases suggest new parallels between the excision reaction performed by transposons of the hAT family and V(D)J recombination. An evaluation of the contribution of small palindromic nucleotide additions produced by transposon excision to the spectrum of spontaneous mutations is also presented.