Jelodar N B, Blackhall N W, Hartman T P, Brar D S, Khush G, Davey M R, Cocking E C, Power J B
Plant Science Division, School of Biological Sciences, University of Nottingham, University Park, Nottingham NG7 2RD, UK, GB.
Theor Appl Genet. 1999 Aug;99(3-4):570-7. doi: 10.1007/s001220051270.
Somatic hybrid plants were obtained following the electrofusion of rice (Oryza sativa L. cv 'Taipei 309', 2n = 2x = 24) cell suspension-derived protoplasts with non-dividing leaf protoplasts of Porteresia coarctata (2n = 4x = 48), a saline-tolerant wild species. Fusion-treated protoplasts were plated on the surface of cellulose nitrate filter membranes, overlaying Lolium multiflorum nurse cells. The nurse cells were embedded in KPR medium containing 0.5 mg l(-1) 2,4-dichlorophenoxyacetic acid and semi-solidified with SeaPlaque agarose. Putative somatic hybrid cell colonies were selected on the basis of their growth, whereby faster growing colonies were transferred preferentially to MS-based medium with 2.0 mg l(-1) kinetin, 0.5 mg l(-1)α-naphthaleneacetic acid, 30 g l(-1) sucrose and 4.0 g l(-1) SeaKem agarose to induce shoot regeneration. One hundred and nineteen regenerated plants were micropropagated clonally on MS-based medium containing 2.0 mg l(-1) 6-benzylaminopurine, 50 g l(-1) sucrose and 4.0 g l(-1) SeaKem agarose, prior to DNA extraction of plant samples. Putative somatic hybrids were initially identified by RAPD analysis, and 8 plant lines were selected for further investigation by flow cytometric ploidy determination and cytology. Plants of one line had an allohexaploid chromosome complement (2n = 6x = 72) and, following examination of its vegetative clones by GISH, were confirmed as somatic hybrids containing full chromosome complements of both O. sativa and P. coarctata.
通过将水稻(Oryza sativa L. cv 'Taipei 309',2n = 2x = 24)细胞悬浮液来源的原生质体与耐盐野生种窄叶泽泻(Porteresia coarctata,2n = 4x = 48)的不分裂叶原生质体进行电融合,获得了体细胞杂种植物。将融合处理后的原生质体接种在硝酸纤维素滤膜表面,覆盖多花黑麦草滋养细胞。滋养细胞包埋于含有0.5 mg l(-1) 2,4 - 二氯苯氧乙酸的KPR培养基中,并用SeaPlaque琼脂糖半固化。根据其生长情况选择推定的体细胞杂种细胞集落,优先将生长较快的集落转移至含有2.0 mg l(-1) 激动素、0.5 mg l(-1) α - 萘乙酸、30 g l(-1) 蔗糖和4.0 g l(-1) SeaKem琼脂糖的MS培养基上诱导芽再生。在对植物样品进行DNA提取之前,将119株再生植株在含有2.0 mg l(-1) 6 - 苄基腺嘌呤、50 g l(-1) 蔗糖和4.0 g l(-1) SeaKem琼脂糖的MS培养基上进行克隆微繁殖。最初通过RAPD分析鉴定推定的体细胞杂种,选择8个株系通过流式细胞术倍性测定和细胞学进行进一步研究。其中一个株系的植物具有异源六倍体染色体组成(2n = 6x = 72),通过基因组原位杂交(GISH)检查其营养克隆后,确认为包含水稻和窄叶泽泻完整染色体组的体细胞杂种。