Yamagishi H., Landgren M., Forsberg J., Glimelius K.
Department of Biotechnology, Kyoto Sangyo University, Kamigamo, Kita, Kyoto 603-8555, Japan,
Theor Appl Genet. 2002 May;104(6-7):959-964. doi: 10.1007/s00122-002-0881-9. Epub 2002 Apr 6.
Application of the protoplast culture method developed for Brassica protoplasts to protoplasts of Arabidopsis thaliana has increased the opportunities for interspecific hybridizations involving Arabidopsis. A more-efficient and much-simpler method was established compared to the earlier-reported protocol developed for A. thaliana protoplasts in which alginate beads were utilized. Mesophyll protoplasts of A. thaliana (ecotypes 'Landsberg erecta' and 'Wassilewskija') were cultured in the modified 8p liquid medium, which had been developed for Brassica protoplasts. For comparison, protoplasts were cultured in sodium alginate beads supplied with B5 medium according to the protocol for A. thaliana. The protoplasts divided with high frequencies in the 8p medium, and calli proliferated more rapidly than in the sodium alginate beads. High frequencies of shoot differentiation and regeneration were observed in calli of both ecotypes, from about 30% in the ecotype 'Wassilewskija' to about 60% for 'Landsberg erecta'. The more-rapidly the calli developed, the higher the regeneration frequencies were. Asymmetric hybrids between A. thaliana and Brassica napus were obtained by treating the protoplasts of A. thaliana with iodoacetamide (IOA) and B. napus protoplasts with UV-irradiation before fusion with polyethylene glycol (PEG). By using the culture procedure developed for Brassica protoplasts, calli developed and plants were regenerated. Although most of the plants regenerated after cell fusion were A. thaliana-like and were judged to be escapes from IOA treatment, more than ten plants showed hybrid features of both morphological and molecular characters. Among the hybrids that have flowered so far, both male-fertile and male-sterile plants have been obtained. Back-crossings to A. thaliana are now in progress as is morphological and molecular characterization of the plants.
将为芸苔属原生质体开发的原生质体培养方法应用于拟南芥原生质体,增加了涉及拟南芥的种间杂交机会。与早期报道的用于拟南芥原生质体的方案(其中使用了藻酸盐珠)相比,建立了一种更高效、更简单的方法。拟南芥(生态型“Landsberg erecta”和“Wassilewskija”)的叶肉原生质体在为芸苔属原生质体开发的改良8p液体培养基中培养。为了进行比较,根据拟南芥的方案,将原生质体培养在供应有B5培养基的海藻酸钠珠中。原生质体在8p培养基中高频分裂,愈伤组织比在海藻酸钠珠中增殖得更快。在两种生态型的愈伤组织中都观察到了高频的芽分化和再生,从“Wassilewskija”生态型的约30%到“Landsberg erecta”的约60%。愈伤组织发育得越快,再生频率就越高。通过在与聚乙二醇(PEG)融合前用碘乙酰胺(IOA)处理拟南芥原生质体和用紫外线照射甘蓝型油菜原生质体,获得了拟南芥和甘蓝型油菜之间的不对称杂种。通过使用为芸苔属原生质体开发的培养程序,愈伤组织得以发育并再生出植株。尽管细胞融合后再生的大多数植株类似拟南芥,被判定为未受IOA处理的逃逸植株,但有十多株表现出形态和分子特征的杂种特性。在目前已开花的杂种中,已获得了雄性可育和雄性不育的植株。目前正在进行与拟南芥的回交以及对这些植株的形态和分子特征鉴定。