Murfett J, Ebert P R, Haring V, Clarke A E
Plant Cell Biology Research Centre, School of Botany, University of Melbourne, Parkville, Victoria, Australia.
Plant Mol Biol. 1995 Aug;28(5):957-63. doi: 10.1007/BF00042080.
Nicotiana tabacum and Nicotiana alata plants were transformed with genomic clones of two S-RNase alleles from N. alata. Neither the S2 clone, with 1.6 kb of 5' sequence, nor the S6 clone, with 2.8 kb of 5' sequence, were expressed at detectable levels in transgenic N. tabacum plants. In N. alata, expression of the S2 clone was not detected, however the S6 clone was expressed (at low levels) in three out of four transgenic plants. An S6-promoter-GUS fusion gene was also expressed in transgenic N. alata but not N. tabacum. Although endogenous S-RNase genes are expressed exclusively in floral pistils, the GUS fusion was expressed in both styles and leaves.
用来自白花烟草的两个S-RNase等位基因的基因组克隆转化了烟草和花烟草植株。具有1.6 kb 5'序列的S2克隆和具有2.8 kb 5'序列的S6克隆在转基因烟草植株中均未检测到可检测水平的表达。在花烟草中,未检测到S2克隆的表达,然而S6克隆在四株转基因植株中的三株中表达(水平较低)。一个S6启动子-GUS融合基因也在转基因花烟草中表达,但在烟草中不表达。尽管内源性S-RNase基因仅在花的雌蕊中表达,但GUS融合基因在花柱和叶片中均有表达。