Drouaud Jan, Camilleri Christine, Bourguignon Pierre-Yves, Canaguier Aurélie, Bérard Aurélie, Vezon Daniel, Giancola Sandra, Brunel Dominique, Colot Vincent, Prum Bernard, Quesneville Hadi, Mézard Christine
Station de Génétique et d'Amélioration des Plantes, Institut Jean-Pierre Bourgin, Institut National de la Recherche Agronomique, 78026, Versailles cedex, France.
Genome Res. 2006 Jan;16(1):106-14. doi: 10.1101/gr.4319006. Epub 2005 Dec 12.
Crossover (CO) is a key process for the accurate segregation of homologous chromosomes during the first meiotic division. In most eukaryotes, meiotic recombination is not homogeneous along the chromosomes, suggesting a tight control of the location of recombination events. We genotyped 71 single nucleotide polymorphisms (SNPs) covering the entire chromosome 4 of Arabidopsis thaliana on 702 F2 plants, representing 1404 meioses and allowing the detection of 1171 COs, to study CO localization in a higher plant. The genetic recombination rates varied along the chromosome from 0 cM/Mb near the centromere to 20 cM/Mb on the short arm next to the NOR region, with a chromosome average of 4.6 cM/Mb. Principal component analysis showed that CO rates negatively correlate with the G+C content (P = 3x10(-4)), in contrast to that reported in other eukaryotes. COs also significantly correlate with the density of single repeats and the CpG ratio, but not with genes, pseudogenes, transposable elements, or dispersed repeats. Chromosome 4 has, on average, 1.6 COs per meiosis, and these COs are subjected to interference. A detailed analysis of several regions having high CO rates revealed "hot spots" of meiotic recombination contained in small fragments of a few kilobases. Both the intensity and the density of these hot spots explain the variation of CO rates along the chromosome.
交换(CO)是第一次减数分裂期间同源染色体精确分离的关键过程。在大多数真核生物中,减数分裂重组在染色体上并非均匀分布,这表明重组事件的位置受到严格控制。我们对702株F2植株的拟南芥第4号染色体上覆盖的71个单核苷酸多态性(SNP)进行了基因分型,代表1404次减数分裂,可检测到1171次交换,以研究高等植物中的交换定位。遗传重组率沿染色体变化,从着丝粒附近的0 cM/Mb到NOR区域旁边短臂上的20 cM/Mb,染色体平均为4.6 cM/Mb。主成分分析表明,与其他真核生物报道的情况相反,交换率与G+C含量呈负相关(P = 3×10⁻⁴)。交换也与单拷贝重复序列的密度和CpG比率显著相关,但与基因、假基因、转座元件或分散重复序列无关。第4号染色体平均每次减数分裂有1.6次交换,并且这些交换受到干扰。对几个具有高交换率区域的详细分析揭示了包含在几千碱基小片段中的减数分裂重组“热点”。这些热点的强度和密度都解释了交换率沿染色体的变化。