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| Centromere targeting; Mutagenesis; Kinetochore; CENH3; Transgenosis; Histone Fold Domain; Loop1 | |
| Eukaryotic chromosomes need centromeres to ensure their faithful transmission to daughter nuclei during nuclear division. The centromere is the site where the kinetochore assembles for chromosome attachment to the spindle microtubules directing the chromosome segregation during nuclear division. Kinetochore assembly requires deposition of the centromeric histone H3 variant (CENH3) into centromeric nucleosomes. CENH3 has a variable N-terminal and a more conserved C-terminal part including the loop1 region of the histone fold domain which is considered to be critical for centromere targeting. To investigate the structural requirements for centromere targeting constructs for tagged CENH3 of A. lyrata A. arenosa Capsella bursa-pastoris Zea mays and Luzula nivea (the latter with holocentric chromosomes) were transformed into A. thaliana. Except for LnCENH3 all recombinant CENH3 proteins targeted A. thaliana centromeres but the more distantly related the alien protein is the lower is the efficiency of targeting. Alignment of CENH3 sequences revealed that the tested species share only three amino acids at loop1 region: threonine (T/2) arginine (R/12) and alanine (A/15). These three amino acids were substituted by asparagine proline and valine encoding sequences within a recombinant EYFP-AtCENH3 construct via PCR mutagenesis prior to transformation of A. thaliana. After transformation immunostaining of root tip nuclei with anti-GFP antibodies yielded only diffuse signals indicating that the original three amino acids are necessary but not sufficient for targeting A. thaliana centromeres. |
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