Kasha K J, Hu T C, Oro R, Simion E, Shim Y S
Department of Plant Agriculture, Biotechnology Division, University of Guelph, Guelph, Ontario, Canada N1G 2W1.
J Exp Bot. 2001 Jun;52(359):1227-38.
A cytological study of barley microspores during pretreatment of the uninucleate stage to the early culture stage was conducted utilizing six genotypes. Among the three main pretreatments investigated, microspores completed the first mitotic division during 28 d cold pretreatment of spikes, with or without leaf sheath attached, and during 0.3 M mannitol pretreatment of anthers at 25 degrees C. However, during a 4 d pretreatment in 0.3 M mannitol at 4 degrees C this first mitotic division was blocked or delayed and subsequently most often occurred during the first day on culture medium. The first mitotic division of most microspores pretreated in 0.3 M mannitol was mostly symmetrical (55-60%), whereas it was asymmetric (94%) during the 28 d cold pretreatment of spikes. Following the first mitotic division during the mannitol pretreatment at 25 degrees C, closely associated daughter nuclei often appeared to fuse via membrane coalescence, leading to a high frequency of large uninucleate microspores. Based upon nuclear size, the frequencies of fused uninucleate microspores in genotypes GBC 778, GBC 777 and Igri were estimated to be 87%, 54% and 75%, respectively, after a 4 d mannitol pretreatment at 25 degrees C. Chromosome numbers in dividing nuclei and relative densitometry measurements of nuclear DNA in microspores from cv. Igri confirmed the apparent fused nature of large nuclei in uninucleate microspores. The high frequency of fused nuclei indicates that nuclear fusion occurred between both symmetric and asymmetric nuclei. Microspores of cv. Igri cultured on filter paper following three different pretreatments provided an average of about 12 000 embryo-like structures (ELS) per plate. In samples, 85-97% of these ELS regenerated green shoots. The frequency of doubled haploids (74-83%) following all pretreatments was similar to the frequencies of fused nuclei. The pretreatment of spikes in 0.3 M mannitol at 4 degrees C for 4 d is preferred as it appears to provide genotype independent induction and suspension of nuclear division, as well as regenerating green plants in a shorter time than cold alone.
利用六个基因型对大麦小孢子从单核期预处理到早期培养阶段进行了细胞学研究。在所研究的三种主要预处理中,小孢子在带或不带叶鞘的穗进行28天低温预处理以及在25℃下用0.3M甘露醇预处理花药期间完成了第一次有丝分裂。然而,在4℃下用0.3M甘露醇进行4天预处理期间,第一次有丝分裂被阻断或延迟,随后大多在培养基上培养的第一天发生。在25℃下用0.3M甘露醇预处理的大多数小孢子的第一次有丝分裂大多是对称的(55 - 60%),而在穗进行28天低温预处理期间则是不对称的(94%)。在25℃下用甘露醇预处理期间第一次有丝分裂之后,紧密相连的子核常常似乎通过膜融合而融合,导致出现高频率的大型单核小孢子。根据核大小,在25℃下用甘露醇进行4天预处理后,基因型GBC 778、GBC 777和Igri中融合单核小孢子的频率估计分别为87%、54%和75%。来自cv. Igri的分裂核中的染色体数以及小孢子中核DNA的相对光密度测量证实了单核小孢子中大型核的明显融合性质。融合核的高频率表明对称核和不对称核之间都发生了核融合。cv. Igri的小孢子在三种不同预处理后在滤纸上培养,每平板平均产生约12000个胚状体结构(ELS)。在样本中,这些ELS中有85 - 97%再生出绿色芽。所有预处理后双单倍体的频率(74 - 83%)与融合核的频率相似。在4℃下用0.3M甘露醇对穗进行4天预处理是优选的,因为它似乎能提供与基因型无关的核分裂诱导和暂停,并且比单独低温处理能在更短时间内再生出绿色植株。