Langston Brennick J, Bai Shuangyi, Jones Michelle L
Department of Horticulture and Crop Science, 1680 Madison Avenue, The Ohio State University, OARDC, Wooster, OH 44691, USA.
J Exp Bot. 2005 Jan;56(409):15-23. doi: 10.1093/jxb/eri002. Epub 2004 Oct 8.
The programmed senescence of flower petals has been shown to involve the fragmentation of nuclear DNA. Nuclear DNA fragmentation, as determined by the TUNEL assay, was detected in Petunia x hybrida corollas during both pollination-induced and age-related senescence. DNA fragmentation was detected late in the lifespan of the flower when corollas were wilting and producing ethylene. The induction of a 43 kDa nuclease (PhNUC1) correlated with increased DNA fragmentation. PhNUC1 is a glycoprotein with activity against DNA and RNA and a pH optimum of 7.5. EDTA was found to inhibit PhNUC1 activity, but the addition of Co2+ restored activity in the presence of the chelating agent. When total protein extracts from senescing petals were fractionated by differential centrifugation, PhNUC1 activity was detected in the nuclear but not the cytoplasmic fraction. Activity of PhNUC1 was induced in non-senescing corollas by treatment with ethylene. Delayed increases in PhNUC1 activity observed in ethylene-insensitive flowers (35S:etr1-1) suggest that ethylene modulates the timing of PhNUC1 induction, but that it is not an absolute requirement for its activation.
花瓣的程序性衰老已被证明与核DNA片段化有关。通过TUNEL分析确定,在矮牵牛杂交种的花冠中,授粉诱导衰老和与年龄相关的衰老过程中均检测到核DNA片段化。当花冠枯萎并产生乙烯时,在花的寿命后期检测到DNA片段化。一种43 kDa核酸酶(PhNUC1)的诱导与DNA片段化增加相关。PhNUC1是一种糖蛋白,对DNA和RNA具有活性,最适pH为7.5。发现EDTA可抑制PhNUC1活性,但在螯合剂存在的情况下添加Co2+可恢复活性。当通过差速离心对衰老花瓣的总蛋白提取物进行分级分离时,在细胞核部分而非细胞质部分检测到PhNUC1活性。用乙烯处理未衰老的花冠可诱导PhNUC1活性。在乙烯不敏感的花朵(35S:etr1-1)中观察到PhNUC1活性延迟增加,这表明乙烯调节PhNUC1诱导的时间,但它不是其激活的绝对必要条件。