Li L, Gerecke E E, Zolan M E
Department of Biology, Indiana University, 1001 East 3rd Street, Bloomington, IN 47405, USA.
Chromosoma. 1999 Nov;108(6):384-92. doi: 10.1007/s004120050390.
We have used fluorescence in situ hybridization to examine homolog pairing during the synchronous meiosis of the basidiomycete Coprinus cinereus. Using spread preparations of meiotic nuclei, we confirmed previous studies that showed that at 6 h post-karyogamy essentially all meiotic nuclei are in pachytene. We found that homolog pairing occurs rapidly after karyogamy, that a 1 Mb chromosome does not associate more quickly than a 2.5 Mb chromosome, and that interstitial, single-copy sites can associate stably prior to nucleolar fusion. Analysis of two probes for the same pair of homologs revealed that by 4 h after karyogamy each chromosome examined was at least partially paired in all meiotic cells. In addition, these studies showed that chromatin condensation increases after pairing and that chromatin shows stable compaction at pachytene.
我们利用荧光原位杂交技术,在担子菌灰盖鬼伞的同步减数分裂过程中检测同源染色体配对情况。通过减数分裂细胞核的涂片制备,我们证实了之前的研究结果,即核融合后6小时,基本上所有减数分裂细胞核都处于粗线期。我们发现同源染色体配对在核融合后迅速发生,1兆碱基对的染色体与2.5兆碱基对的染色体配对速度并无差异,并且在核仁融合之前,染色体间的单拷贝位点能够稳定配对。对同一对同源染色体的两个探针进行分析发现,核融合后4小时,在所有减数分裂细胞中,每条被检测的染色体至少部分配对。此外,这些研究表明,配对后染色质凝聚增加,并且在粗线期染色质呈现稳定的压缩状态。