RICE TYPE-I PHYTOCHROME REGULATES HYPOCOTYL ELONGATION IN TRANSGENIC TOBACCO SEEDLINGS

被引:62
作者
NAGATANI, A [1 ]
KAY, SA [1 ]
DEAK, M [1 ]
CHUA, NH [1 ]
FURUYA, M [1 ]
机构
[1] ROCKEFELLER UNIV,PLANT MOLEC BIOL LAB,NEW YORK,NY 10021
关键词
LIGHT REGULATION; TRANSGENIC PLANTS; PLANT DEVELOPMENT; GROWTH REGULATION;
D O I
10.1073/pnas.88.12.5207
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have examined the biological activity of rice type I phytochrome (PI) in transgenic tobacco seedlings. The progeny of four independent transformants that expressed the rice PI gene segregated 3:1 for shorter hypocotyl length under dim white light (0.04 W/m2). By contrast, this phenotype was not observed either in the dark or under white light at higher intensity (6.0 W/m2). This suggests that the phenotype is dependent not only on light but also on light intensity. The increased light sensitivity cosegregated with the kanamycin-resistance marker as well as with the rice PI polypeptides, indicating that this phenotype is directly related to the expression of the transgene. The transgenic plants showing short hypocotyls exhibited a reduced growth rate throughout the elongation period, and the resulting shorter hypocotyl length was attributable to shorter epidermal cell length but not to reduced cell number. Furthermore, successive pulse irradiations with red light elicited short hypocotyls similar to those obtained under dim white light, and the effect was reversed by immediate far-red light treatment, providing a direct indication that the phenotype is caused by biologically active rice PI. Therefore, the far-red-absorbing form of the introduced rice PI appears to regulate the hypocotyl length of the transgenic tobacco plants through endogenous signal-transduction pathways. This assay system will be a powerful tool for testing the biological activity of introduced phytochrome molecules.
引用
收藏
页码:5207 / 5211
页数:5
相关论文
共 22 条
[1]  
ABE H, 1985, PLANT CELL PHYSIOL, V26, P1387
[2]   AMINO-TERMINAL AMINO-ACID-SEQUENCES OF PEA PHYTOCHROME-II FRAGMENTS OBTAINED BY LIMITED PROTEOLYSIS [J].
ABE, H ;
TAKIO, K ;
TITANI, K ;
FURUYA, M .
PLANT AND CELL PHYSIOLOGY, 1989, 30 (08) :1089-1097
[3]   REGULATED GENES IN TRANSGENIC PLANTS [J].
BENFEY, PN ;
CHUA, NH .
SCIENCE, 1989, 244 (4901) :174-181
[4]  
BOYLAN MT, 1989, PLANT CELL, V1, P765, DOI 10.1105/tpc.1.8.765
[5]   DETECTION, ASSAY, AND PRELIMINARY PURIFICATION OF THE PIGMENT CONTROLLING PHOTORESPONSIVE DEVELOPMENT OF PLANTS [J].
BUTLER, WL ;
NORRIS, KH ;
SIEGELMAN, HW ;
HENDRICKS, SB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1959, 45 (12) :1703-1708
[6]   ELECTRON-MICROSCOPIC LOCALIZATION OF PHYTOCHROME IN PLANTS USING AN INDIRECT ANTIBODY-LABELING METHOD [J].
COLEMAN, RA ;
PRATT, LH .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1974, 22 (11) :1039-1047
[7]  
Furuya M, 1989, Adv Biophys, V25, P133, DOI 10.1016/0065-227X(89)90006-3
[8]  
FURUYA M, 1987, PHYTOCHROME PHOTOREG, P354
[9]   MOLECULAR LIGHT SWITCHES FOR PLANT GENES [J].
GILMARTIN, PM ;
SAROKIN, L ;
MEMELINK, J ;
CHUA, NH .
PLANT CELL, 1990, 2 (05) :369-378
[10]  
KAY SA, 1989, PLANT CELL, V1, P775, DOI 10.1105/tpc.1.8.775