Abstract
We have compared a total of 30 recognition sites for eight restriction endonucleases on the 20-kilobase-pair maxi-circle of kinetoplast DNAs from five different Trypanosoma brucei strains. In addition to three polymorphic sites we have found a 5 kilobase-pair region that is not cleaved by any of the eight enzymes and that varies in size over 1 kilobase pair in the strains analysed. Mini-circles from these five strains, digested with endonuclease TaqI or MboII, yield very complex fragment patterns, showing that extensive mini-circle sequence heterogeneity is a common characteristic of these T. brucei strains. The size distribution of mini-circle fragments in these digests was identical for different clones of the 427 strain, but very different for mini-circles from different strains. These results show that maxi-circle sequence is conserved, whereas mini-circle sequence is not. Restriction digests of maxi-circles could be useful in determining how closely two Trypanosoma strains are related, whereas mini-circle digests can serve as sensitive tags for individual strains.
| Original language | English |
|---|---|
| Pages (from-to) | 197-210 |
| Number of pages | 14 |
| Journal | BBA Section Nucleic Acids And Protein Synthesis |
| Volume | 610 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 11 Dec 1980 |
| Externally published | Yes |
Keywords
- (Trypanosoma brucei)
- Maxi-circle
- Mini-circle
- Nucleotide sequence
- Restriction endonuclease
- kinetoplast DNA
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