Oh S A, Lee S Y, Chung I K, Lee C H, Nam H G
Department of Life Science, Pohang University of Science and Technology, Kyungbuk, South Korea.
Plant Mol Biol. 1996 Feb;30(4):739-54. doi: 10.1007/BF00019008.
We have characterized the structure and expression of a senescence-associated gene (sen1) of Arabidopsis thaliana. The protein-coding region of the gene consists of 5 exons encoding 182 amino acids. The encoded peptide shows noticeable similarity to the bacterial sulfide dehydrogenase and 81% identity to the peptide encoded by the radish din1 gene. The 5'-upstream region contains sequence motifs resembling the heat-shock- and ABA-responsive elements and the TCA motif conserved among stress-inducible genes. Examination of the expression patterns of the sen1 gene under various senescing conditions along with measurements of photochemical efficiency and of chlorophyll content revealed that the sen1 gene expression is associated with Arabidopsis leaf senescence. During the normal growth phase, the gene is strongly induced in leaves at 25 days after germination when inflorescence stems are 2-3 cm high, and then the mRNA level is maintained at a comparable level in naturally senescing leaves. In addition, dark-induced senescence of detached leaves or of leaves in planta resulted in a high-level induction of the gene. Expression of the sen1 gene was also strongly induced in leaves subjected to senescence by 0.1mM abscisic acid or 1 mM ethephon treatment. The induced expression of the gene by dark treatment was not significantly repressed by treatment with 0.1 mM cytokinin or 50 mM CaCl2 which delayed loss of chlorophyll but not that of photochemical efficiency.
我们已经对拟南芥衰老相关基因(sen1)的结构和表达进行了表征。该基因的蛋白质编码区由5个外显子组成,编码182个氨基酸。编码的肽段与细菌硫化物脱氢酶有明显的相似性,与萝卜din1基因编码的肽段有81%的同一性。5'上游区域包含类似于热休克和脱落酸应答元件的序列基序以及应激诱导基因中保守的TCA基序。对sen1基因在各种衰老条件下的表达模式进行检测,并同时测量光化学效率和叶绿素含量,结果表明sen1基因的表达与拟南芥叶片衰老相关。在正常生长阶段,该基因在萌发后25天、花序茎高2 - 3厘米时在叶片中强烈诱导表达,然后在自然衰老的叶片中mRNA水平维持在相当的水平。此外,离体叶片或植株上叶片的黑暗诱导衰老导致该基因的高水平诱导表达。用0.1 mM脱落酸或1 mM乙烯利处理使叶片衰老时,sen1基因的表达也强烈诱导。黑暗处理诱导的该基因表达不会被0.1 mM细胞分裂素或50 mM氯化钙处理显著抑制,这两种处理延缓了叶绿素的损失,但没有延缓光化学效率的损失。