Abstract
Phytophthora infestans is the cause of late blight, a devastating and re-emerging disease of potato. Significant advances have been made in understanding the biology of P. infestans, and in the development of molecular tools to study this oomycete. Nevertheless, little is known about the molecular bases of the establishment or development of disease in this hemibiotrophic pathogen. Suppression subtractive hybridization (SSH) was used to generate cDNA enriched for sequences upregulated during potato infection. To identify pathogen-derived cDNAs, and eliminate host sequences from further study, SSH cDNA was hybridized to a P. infestans bacterial artificial chromosome library. A new gene family was identified called Pinci1, comprising more than 400 members arranged in clusters of up to nine copies throughout the P. infestans draft genome sequence. Real-time RT-PCR was used to quantify the expression of five classes of transcript within the family, relative to the constitutively expressed PiactA gene, and it revealed them to be significantly upregulated from 12 to 33 h post-inoculation, a period defining the biotrophic phase of infection. Computational analysis of sequences suggested that transcripts were non-protein coding, and this was confirmed by transient expression of FLAG-tagged ORFs in P. infestans.
Original language | English |
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Pages (from-to) | 747-759 |
Number of pages | 13 |
Journal | Microbiology |
Volume | 153 |
Issue number | Pt 3 |
DOIs | |
Publication status | Published - 1 Mar 2007 |
Keywords
- Base Sequence
- DNA, Algal/chemistry
- Gene Dosage
- Gene Expression Profiling
- Gene Expression Regulation
- Gene Library
- Genome
- Molecular Sequence Data
- Phytophthora/cytology
- RNA, Algal/analysis
- RNA, Untranslated/genetics
- Reverse Transcriptase Polymerase Chain Reaction
- Solanum tuberosum/microbiology