Miller J D, Arteca R N, Pell E J
Intercollege Graduate Program in Plant Physiology, The Pennsylvania State University, University Park 16802, USA.
Plant Physiol. 1999 Aug;120(4):1015-24. doi: 10.1104/pp.120.4.1015.
The expression patterns of senescence-related genes were determined during ozone (O(3)) exposure in Arabidopsis. Rosettes were treated with 0.15 microL L(-1) O(3) for 6 h d(-1) for 14 d. O(3)-treated leaves began to yellow after 10 d of exposure, whereas yellowing was not apparent in control leaves until d 14. Transcript levels for eight of 12 senescence related genes characterized showed induction by O(3). SAG13 (senescence-associated gene), SAG21, ERD1 (early responsive to dehydration), and BCB (blue copper-binding protein) were induced within 2 to 4 d of O(3) treatment; SAG18, SAG20, and ACS6 (ACC synthase) were induced within 4 to 6 d; and CCH (copper chaperone) was induced within 6 to 8 d. In contrast, levels of photosynthetic gene transcripts, rbcS (small subunit of Rubisco) and cab (chlorophyll a/b-binding protein), declined after 6 d. Other markers of natural senescence, SAG12, SAG19, MT1 (metallothionein), and Atgsr2 (glutamine synthetase), did not show enhanced transcript accumulation. When SAG12 promoter-GUS (beta-glucuronidase) and SAG13 promoter-GUS transgenic plants were treated with O(3), GUS activity was induced in SAG13-GUS plants after 2 d but was not detected in SAG12-GUS plants. SAG13 promoter-driven GUS activity was located throughout O(3)-treated leaves, whereas control leaves generally showed activity along the margins. The acceleration of leaf senescence induced by O(3) is a regulated event involving many genes associated with natural senescence.
在拟南芥暴露于臭氧(O₃)期间,测定衰老相关基因的表达模式。莲座叶用0.15 μL L⁻¹ O₃处理,每天处理6小时,持续14天。暴露10天后,经O₃处理的叶片开始变黄,而对照叶片直到第14天才出现明显变黄。所鉴定的12个衰老相关基因中的8个基因的转录水平显示受到O₃诱导。衰老相关基因13(SAG13)、衰老相关基因21(SAG21)、脱水早期响应基因1(ERD1)和蓝铜结合蛋白(BCB)在O₃处理2至4天内被诱导;衰老相关基因18(SAG18)、衰老相关基因20(SAG20)和乙烯合成酶6(ACS6)在4至6天内被诱导;而铜伴侣蛋白(CCH)在6至8天内被诱导。相比之下,光合基因转录本,即核酮糖-1,5-二磷酸羧化酶小亚基(rbcS)和叶绿素a/b结合蛋白(cab)的水平在6天后下降。自然衰老的其他标记物,衰老相关基因12(SAG12)、衰老相关基因19(SAG19)、金属硫蛋白1(MT1)和谷氨酰胺合成酶(Atgsr2),未显示转录积累增强。当用O₃处理衰老相关基因12启动子 - β-葡萄糖醛酸酶(GUS)和衰老相关基因13启动子 - GUS转基因植物时,GUS活性在衰老相关基因13 - GUS植物中2天后被诱导,但在衰老相关基因12 - GUS植物中未检测到。衰老相关基因13启动子驱动的GUS活性位于整个经O₃处理的叶片中,而对照叶片通常仅在叶缘显示活性。O₃诱导的叶片衰老加速是一个涉及许多与自然衰老相关基因的调控过程。