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通过微粒轰击产生的转基因植物的分子分析:矮牵牛转化增强序列的作用

Molecular analysis of transgenic plants generated by microprojectile bombardment: effect of petunia transformation booster sequence.

作者信息

Buising C M, Benbow R M

机构信息

Department of Zoology and Genetics, Iowa State University, Ames 50011-3223.

出版信息

Mol Gen Genet. 1994 Apr;243(1):71-81. doi: 10.1007/BF00283878.

DOI:10.1007/BF00283878
PMID:8190073
Abstract

Supercoiled plasmid expression vectors containing the petunia transformation booster sequence (TBS) were introduced by microprojectile bombardment into dicotyledenous (tobacco) and monocotyledonous (maize) cells. TBS effected a 7.8- to 16-fold increase in transformation frequencies in tobacco, and a 1.7- to 2.4-fold increase in maize. Although TBS contains a well-defined transcription enhancer element, no increases in plasmid gene expression were observed. TBS did not alter integration patterns in transformants, and did not affect segregation of linkage in R1 progeny. Computer analyses of the TBS sequence revealed numerous modular elements previously shown to be associated with putative chromosomal replication origin regions in eukaryotes, including DNA unwinding elements, scaffold-associated regions and pyrimidine tracts.

摘要

含有矮牵牛转化增强序列(TBS)的超螺旋质粒表达载体通过微粒轰击法导入双子叶植物(烟草)和单子叶植物(玉米)细胞中。TBS使烟草的转化频率提高了7.8至16倍,使玉米的转化频率提高了1.7至2.4倍。尽管TBS含有一个明确的转录增强元件,但未观察到质粒基因表达增加。TBS未改变转化体中的整合模式,也不影响R1后代中连锁的分离。对TBS序列的计算机分析揭示了许多先前显示与真核生物中假定的染色体复制起始区域相关的模块化元件,包括DNA解旋元件、支架相关区域和嘧啶序列。

相似文献

1
Molecular analysis of transgenic plants generated by microprojectile bombardment: effect of petunia transformation booster sequence.通过微粒轰击产生的转基因植物的分子分析:矮牵牛转化增强序列的作用
Mol Gen Genet. 1994 Apr;243(1):71-81. doi: 10.1007/BF00283878.
2
Segregation of transgenes in maize.玉米中转基因的分离
Plant Mol Biol. 1992 Jan;18(2):201-10. doi: 10.1007/BF00034949.
3
Transposition of the maize autonomous element Activator in transgenic Nicotiana plumbaginifolia plants.玉米自主元件激活子在转基因白花烟草植株中的转座
Mol Gen Genet. 1993 Apr;238(1-2):209-17. doi: 10.1007/BF00279549.
4
A genomic DNA segment from Petunia hybrida leads to increased transformation frequencies and simple integration patterns.来自矮牵牛的一个基因组DNA片段可提高转化频率并产生简单的整合模式。
Proc Natl Acad Sci U S A. 1988 Nov;85(22):8568-72. doi: 10.1073/pnas.85.22.8568.
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Presence of an SAR-like sequence in junction regions between an introduced transgene and genomic DNA of cultured tobacco cells: its effect on transformation frequency.在导入的转基因与培养烟草细胞基因组DNA的连接区域中存在类SAR序列:其对转化频率的影响。
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The maize transposable element Ac excises in progeny of transformed tobacco.玉米转座因子Ac在转基因烟草的后代中发生切除。
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Transgenic tobacco plants and their progeny derived by microprojectile bombardment of tobacco leaves.通过微弹轰击烟草叶片获得的转基因烟草植株及其后代。
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Intrachromosomal recombination between attP regions as a tool to remove selectable marker genes from tobacco transgenes.attP区域间的染色体内重组作为从烟草转基因中去除选择标记基因的一种工具。
Nat Biotechnol. 2000 Apr;18(4):442-5. doi: 10.1038/74515.
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Induced transposition of Ds by a stable Ac in crosses of transgenic tobacco plants.在转基因烟草植株杂交中,由稳定的Ac诱导Ds转座。
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Preferential transposition of the maize element Activator to linked chromosomal locations in tobacco.玉米激活子元件在烟草中优先转座至连锁的染色体位点。
Plant Cell. 1990 Aug;2(8):701-7. doi: 10.1105/tpc.2.8.701.

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A transformation booster sequence (TBS) from Petunia hybrida functions as an enhancer-blocking insulator in Arabidopsis thaliana.

本文引用的文献

1
Effect of repeated DNA sequences on direct gene transfer in protoplasts of Nicotiana plumbaginifolia.重复 DNA 序列对烟草原生质体直接基因转移的影响。
Theor Appl Genet. 1989 Jul;78(1):113-8. doi: 10.1007/BF00299763.
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Duplication of CaMV 35S Promoter Sequences Creates a Strong Enhancer for Plant Genes.CaMV 35S 启动子序列的重复产生了植物基因的强启动子。
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Transformation of Brassica napus and Brassica oleracea Using Agrobacterium tumefaciens and the Expression of the bar and neo Genes in the Transgenic Plants.
来自矮牵牛的转化增强子序列(TBS)在拟南芥中作为增强子阻断绝缘子发挥作用。
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The transformation booster sequence from Petunia hybrida is a retrotransposon derivative that binds to the nuclear scaffold.矮牵牛的转化增强序列是一种与核支架结合的逆转座子衍生物。
Mol Gen Genet. 1995 Jun 10;247(5):614-22. doi: 10.1007/BF00290353.
利用根癌农杆菌对甘蓝型油菜和甘蓝进行转化以及转基因植株中bar和neo基因的表达
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Proc Natl Acad Sci U S A. 1988 Nov;85(22):8502-5. doi: 10.1073/pnas.85.22.8502.
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Transfer of foreign genes into intact maize cells with high-velocity microprojectiles.利用高速微弹将外源基因导入完整的玉米细胞。
Proc Natl Acad Sci U S A. 1988 Jun;85(12):4305-9. doi: 10.1073/pnas.85.12.4305.
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Gene targeting in plants.植物基因靶向。
EMBO J. 1988 Dec 20;7(13):4021-6. doi: 10.1002/j.1460-2075.1988.tb03295.x.
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Characterization of the herbicide-resistance gene bar from Streptomyces hygroscopicus.从吸水链霉菌中鉴定出除草剂抗性基因 bar。
EMBO J. 1987 Sep;6(9):2519-23. doi: 10.1002/j.1460-2075.1987.tb02538.x.
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Engineering herbicide resistance in plants by expression of a detoxifying enzyme.通过表达解毒酶来工程植物的抗除草剂性。
EMBO J. 1987 Sep;6(9):2513-8. doi: 10.1002/j.1460-2075.1987.tb02537.x.
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Scaffold attachment regions increase reporter gene expression in stably transformed plant cells.支架附着区域可提高稳定转化植物细胞中报告基因的表达。
Plant Cell. 1993 Jun;5(6):603-13. doi: 10.1105/tpc.5.6.603.
10
"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.一种将DNA限制性内切酶片段放射性标记至高比活度的技术。附录
Anal Biochem. 1984 Feb;137(1):266-7. doi: 10.1016/0003-2697(84)90381-6.