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水稻[亚洲栽培稻(Oryza sativa L.)(+) 窄叶野生稻(Porteresia coarctata (Roxb.) Tateoka)]的属间体细胞杂种。

Intergeneric somatic hybrids of rice [Oryza sativa L. (+) Porteresia coarctata (Roxb.) Tateoka].

作者信息

Jelodar N B, Blackhall N W, Hartman T P, Brar D S, Khush G, Davey M R, Cocking E C, Power J B

机构信息

Plant Science Division, School of Biological Sciences, University of Nottingham, University Park, Nottingham NG7 2RD, UK, GB.

出版信息

Theor Appl Genet. 1999 Aug;99(3-4):570-7. doi: 10.1007/s001220051270.

Abstract

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.

摘要

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。

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