Ko Tae-Seok, Lee Sangman, Farrand Stephen K, Korban Schuyler S
Department of Natural Resources and Environmental Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Planta. 2004 Feb;218(4):536-41. doi: 10.1007/s00425-003-1135-z. Epub 2003 Nov 14.
Agrobacterium tumefaciens strain KYRT1 harboring the virulence helper plasmid pKYRT1 induces transgenic somatic embryos (SEs) at high frequency from infected immature soybean cotyledons. KYRT1 is derived from the highly oncogenic strain Chry5. However, pKYRT1 is not completely disarmed and still contains an entire T-right (T(R)) and a portion of T-left (T(L)). In this report, binary strains, each carrying fully disarmed vir helper plasmids including pKPSF2, which is a fully disarmed version of pKYRT1, were compared to strain KYRT1 for their ability to induce transgenic SEs on immature cotyledons of soybean. Six weeks following cocultivation, histochemical GUS assays of cultured explants indicated that all fully disarmed vir helper plasmids transferred their binary T-DNA, containing a GUS-intron gene, into soybean tissues. However, none of these transformed tissues developed SEs on medium with or without 2,4-dichlorophenoxyactic acid (2,4-D). On the other hand, immature cotyledons cocultivated with strain KYRT1 exhibited high induction of transgenic SEs, but only on medium supplemented with 2,4-D. Derivatives of strain Chry5 harboring other vir helper plasmids did not induce transgenic SEs under any conditions tested, thus suggesting that the chromosomal background of KYRT1 alone was not sufficient to promote somatic embryogenesis. PCR analysis indicated that 55% of transgenic embryogenic cultures and 29% of transgenic T(0) soybean plants derived by transformation using strain KYRT1 contained T(R) from pKYRT1 in addition to the uidA gene from the binary construct. None of the transgenic tissues or T(0) plants contained T(L) DNA. These results suggest that some function coded for by T(R) of pKYRT1 influences somatic embryogenesis in conjunction with exposure of the plant tissues to 2,4-D. Since the co-transformation frequency of the undesirable T-DNA sequences from the vir helper plasmid was relatively low, the partially disarmed strain KYRT1 will likely be very useful for the production of normal transgenic plants of diverse soybean cultivars.
携带毒力辅助质粒pKYRT1的根癌农杆菌菌株KYRT1能以高频率从受感染的未成熟大豆子叶诱导产生转基因体细胞胚(SEs)。KYRT1源自高致癌性菌株Chry5。然而,pKYRT1并未完全解除武装,仍包含完整的T-右(T(R))和部分T-左(T(L))。在本报告中,将携带完全解除武装的毒力辅助质粒(包括pKPSF2,它是pKYRT1的完全解除武装版本)的二元菌株与菌株KYRT1在未成熟大豆子叶上诱导转基因SEs的能力进行了比较。共培养六周后,对外植体进行组织化学GUS分析表明,所有完全解除武装的毒力辅助质粒都将其包含GUS-内含子基因的二元T-DNA转移到了大豆组织中。然而,这些转化组织在添加或不添加2,4-二氯苯氧乙酸(2,4-D)的培养基上均未发育成SEs。另一方面,与菌株KYRT1共培养的未成熟子叶表现出转基因SEs的高诱导率,但仅在添加2,4-D的培养基上。携带其他毒力辅助质粒的Chry5菌株衍生物在任何测试条件下均未诱导出转基因SEs,因此表明仅KYRT1的染色体背景不足以促进体细胞胚胎发生。PCR分析表明,通过使用菌株KYRT1转化获得的55%的转基因胚性培养物和29%的转基因T(0)大豆植株除了含有二元构建体中的uidA基因外,还含有来自pKYRT1的T(R)。转基因组织或T(0)植株均未含有T(L) DNA。这些结果表明,pKYRT1的T(R)编码的某些功能与植物组织暴露于2,4-D共同影响体细胞胚胎发生。由于来自毒力辅助质粒的不良T-DNA序列的共转化频率相对较低,部分解除武装的菌株KYRT1可能对多种大豆品种正常转基因植株的生产非常有用。