Kawabe Akira, Hansson Bengt, Forrest Alan, Hagenblad Jenny, Charlesworth Deborah
Institute of Evolutionary Biology, University of Edinburgh, Ashworth Laboratories King's Buildings, West Mains Road, Edinburgh EH9 3JT, UK.
Genet Res. 2006 Aug;88(1):45-56. doi: 10.1017/S0016672306008287.
We have increased the density of genetic markers on the Arabidopsis lyrata chromosomes AL6 and AL7 corresponding to the A. thaliana chromosome IV, in order to determine chromosome rearrangements between these two species, and to compare recombination fractions across the same intervals. We confirm the two rearrangements previously inferred (a reciprocal translocation and a large inversion, which we infer to be pericentric). By including markers around the centromere regions of A. thaliana chromosomes IV and V, we localize the AL6 centromere, and can localize the breakpoints of these chromosome rearrangements more precisely than previously. One translocation breakpoint was close to the centromere, and the other coincided with one end of the inversion, suggesting that a single event caused both rearrangements. At the resolution of our mapping, apart from these rearrangements, all other markers are in the same order in A. lyrata and A. thaliana. We could thus compare recombination rates in the two species. We found slightly higher values in A. thaliana, and a minimum estimate for regions not close to a centromere in A. lyrata is 4-5 centimorgans per megabase. The mapped region of AL7 includes the self-incompatibility loci (S-loci), and this region has been predicted to have lower recombination than elsewhere in the genome. We mapped 17 markers in a region of 1.23 Mb surrounding these loci, and compared the approximately 600 kb closest to the S-loci with the surrounding region of approximately the same size. There were significantly fewer recombination events in the closer than the more distant region, supporting the above prediction, but showing that the low recombination region is very limited in size.
我们增加了琴叶拟南芥(Arabidopsis lyrata)中与拟南芥(A. thaliana)第四条染色体相对应的AL6和AL7染色体上的遗传标记密度,以确定这两个物种之间的染色体重排,并比较相同区间内的重组率。我们证实了之前推断出的两个重排(一个相互易位和一个大的倒位,我们推断为臂间倒位)。通过在拟南芥第四条和第五条染色体的着丝粒区域周围加入标记,我们定位了AL6着丝粒,并且能够比以前更精确地定位这些染色体重排的断点。一个易位断点靠近着丝粒,另一个与倒位的一端重合,这表明单个事件导致了这两个重排。在我们的定位分辨率下,除了这些重排之外,所有其他标记在琴叶拟南芥和拟南芥中的顺序相同。因此,我们可以比较这两个物种中的重组率。我们发现在拟南芥中的值略高,并且琴叶拟南芥中不靠近着丝粒区域的最小估计值是每兆碱基4 - 5厘摩。AL7的定位区域包括自交不亲和位点(S - 位点),并且该区域预计重组率低于基因组中的其他区域。我们在围绕这些位点的1.23 Mb区域内定位了17个标记,并将最接近S - 位点的约600 kb区域与大小大致相同的周围区域进行了比较。较近区域的重组事件明显少于较远区域,这支持了上述预测,但表明低重组区域的大小非常有限。