Translation from nonautonomous type IAP retrotransposon is a critical determinant of transposition activity: Implication for retrotransposon-mediated genome evolution

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 2.
Figure 2.

Amino acid changes and schematic diagram of the protein structure of mutant IAP vectors. Mutated sites and their effect on protein structure in full-length type (A) and IΔ1 type (B) IAP vectors are depicted. (A) In pFL-M1 and -M2, the first ATG and both the first and the second ATG are disrupted (indicated by ‡), respectively: pFL-M1 generates IAP protein lacking N-terminal 15 amino acids, and pFL-M2 does not generate IAP protein. Premature termination codons are introduced in pFL-M3 to pFL-M5 to truncate the IAP proteins. Gray boxes indicate predicted protein coding regions. (B) A premature termination codon is introduced in pDE1-M3 and pDE1-M11. In pDE1-M6, both the first and the second ATG are disrupted (indicated by ‡). A cluster of basic amino acids is mutated in pDE1-M12. WT, wild type. Details of mutation sites are shown in Supplemental Figures 1 and 2.

This Article

  1. Genome Res. 18: 859-868

Preprint Server