Glyn M C, Egertová M, Gazdova B, Kovarik A, Bezdek M, Leitch A R
School of Biological Sciences, Queen Mary and Westfield College, Mile End Road, London E1 4NS, UK.
Chromosoma. 1997 Dec;106(8):485-92. doi: 10.1007/pl00007688.
This paper describes the effects of 5-azacytidine on the condensation state of rye (Secale cereale L.) chromatin introduced into the wheat genome (Triticum aestivum L. cv. Beaver). The wheat cultivar Beaver carries a translocation between the short arm of rye chromosome 1R (1RS) and the long arm of wheat chromosome 1B (1BL/1RS). 1RS can be detected using genomic in situ hybridisation and carries a ribosomal DNA (rDNA) locus that can be simultaneously detected using multiple labelling strategies. The rDNA locus divides 1RS into a distal region that is gene rich and a proximal region that is gene poor and highly methylated. 1RS also carries a large block of subtelomeric heterochromatin. The drug, which acts to inhibit DNA methylation in plants, has three pronounced effects on interphase nuclei. (1) It induces aberrant condensation of the rye subtelomeric heterochromatin and in many cases induces sister chromatid separation in the subtelomeric heterochromatin of G2 nuclei. (2) Nuclei trisomic for 1RS are observed at low frequency in treated material and are probably a consequence of aberrant sister chromatid separation or condensation. (3) The drug alters normal condensation of 1RS euchromatin. However, contrary to expectation the effect is not simply to induce decondensation. The proximal region of the arm actually condenses at low levels of drug administration while the distal region remains unaltered or increases its decondensation state. Increasing the concentration of 5-azacytidine induces a biphasic response and at the highest concentration used all regions of the arm show signs of decondensation. Thus the influence of the drug on chromatin condensation depends on the genomic structure.
本文描述了5-氮杂胞苷对导入小麦基因组(普通小麦品种Beaver)的黑麦(黑麦草)染色质凝聚状态的影响。小麦品种Beaver在黑麦1R染色体短臂(1RS)和小麦1B染色体长臂(1BL/1RS)之间存在易位。1RS可通过基因组原位杂交检测到,并且携带一个核糖体DNA(rDNA)位点,该位点可使用多种标记策略同时检测。rDNA位点将1RS分为富含基因的远端区域和基因贫乏且高度甲基化的近端区域。1RS还携带一大块亚端粒异染色质。这种作用于抑制植物DNA甲基化的药物对间期核有三种显著影响。(1)它诱导黑麦亚端粒异染色质异常凝聚,在许多情况下还诱导G2期细胞核亚端粒异染色质中的姐妹染色单体分离。(2)在处理过的材料中低频观察到1RS三体细胞核,这可能是异常姐妹染色单体分离或凝聚的结果。(3)该药物改变了1RS常染色质的正常凝聚。然而,与预期相反,其作用并非简单地诱导解聚。在低剂量药物处理时,臂的近端区域实际上会凝聚,而远端区域保持不变或增加其解聚状态。增加5-氮杂胞苷的浓度会诱导双相反应,在使用的最高浓度下,臂的所有区域都显示出解聚迹象。因此,药物对染色质凝聚的影响取决于基因组结构。