期刊文献+

Induced Deactivation of Genes Encoding Chlorophyll Biosynthesis Enzymes Disentangles Tetrapyrrole- Mediated Retrograde Signaling 被引量:3

Induced Deactivation of Genes Encoding Chlorophyll Biosynthesis Enzymes Disentangles Tetrapyrrole- Mediated Retrograde Signaling
原文传递
导出
摘要 In photosynthetic organisms, tetrapyrrole-mediated retrograde signals are proposed to contribute to a bal- anced nuclear gene expression (NGE) in response to metabolic activity in chloroplasts. We followed an experimental short- term approach that allowed the assessment of modified NGE during the first hours of specifically modified enzymatic steps of the Mg branch of tetrapyrrole biosynthesis, when pleiotropic effects of other signals can be avoided. In response to 24-h-induced silencing of CHLH, CHLM, and CHL27 encoding the CHLH subunit of Mg chelatase, the Mg protoporphyrin methyltransferase and Mg protoporphyrin monomethylester cyclase, respectively, deactivated gene expression rapidly led to reduced activity of the corresponding enzymes and altered Mg porphyrin levels. But NGE was not substantially altered. When these three genes were continuously inactivated for up to 4 d, changes of transcript levels of nuclear genes were determined. CHL27 silencing for more than 24h results in necrotic leaf lesions and modulated transcript levels of oxidative stress-responsive and photosynthesis-associated nuclear genes (PhANGs). The prolonged deactivation of CHLH and CHLM results in slightly elevated transcript levels of PhANGs and tetrapyrrole-associated genes. These time-resolved studies indicate a complex scenario for the contribution of tetrapyrrole biosynthesis on NGE mediated by IO2-induced signaling and feedback-regulated ALA synthesis. In photosynthetic organisms, tetrapyrrole-mediated retrograde signals are proposed to contribute to a bal- anced nuclear gene expression (NGE) in response to metabolic activity in chloroplasts. We followed an experimental short- term approach that allowed the assessment of modified NGE during the first hours of specifically modified enzymatic steps of the Mg branch of tetrapyrrole biosynthesis, when pleiotropic effects of other signals can be avoided. In response to 24-h-induced silencing of CHLH, CHLM, and CHL27 encoding the CHLH subunit of Mg chelatase, the Mg protoporphyrin methyltransferase and Mg protoporphyrin monomethylester cyclase, respectively, deactivated gene expression rapidly led to reduced activity of the corresponding enzymes and altered Mg porphyrin levels. But NGE was not substantially altered. When these three genes were continuously inactivated for up to 4 d, changes of transcript levels of nuclear genes were determined. CHL27 silencing for more than 24h results in necrotic leaf lesions and modulated transcript levels of oxidative stress-responsive and photosynthesis-associated nuclear genes (PhANGs). The prolonged deactivation of CHLH and CHLM results in slightly elevated transcript levels of PhANGs and tetrapyrrole-associated genes. These time-resolved studies indicate a complex scenario for the contribution of tetrapyrrole biosynthesis on NGE mediated by IO2-induced signaling and feedback-regulated ALA synthesis.
出处 《Molecular Plant》 SCIE CAS CSCD 2014年第7期1211-1227,共17页 分子植物(英文版)
关键词 plastid signal transcription analysis retrograde signal tetrapyrrole metabolism Mg protoporphyrin. plastid signal transcription analysis retrograde signal tetrapyrrole metabolism Mg protoporphyrin.
  • 相关文献

参考文献3

二级参考文献211

  • 1SarahMMense.Heme:a versatile signaling molecule controlling the activities of diverse regulators ranging from transcription factors to MAP kinases[J].Cell Research,2006,16(8):681-692. 被引量:6
  • 2Lange, B.M., and Ghassemian, M. (2003). Genome organization in Arabidopsis thaliana: a survey for genes involved in isoprenoid and chlorophyll metabolism. Plant Mol. Biol. 51,925-948.
  • 3Lange, B.M., and Ghassemian, M. (2005). Comprehensive post-genomic data analysis approaches integrating biochemical pathway maps. Phytochemistry. 66, 413-451.
  • 4Larkin, R.M., Alonso, J.M., Ecker, J.R., and Chory, J. (2003). GUN4, a regulator of chlorophyll synthesis and intracellular signalling. Science. 299, 902-906.
  • 5Li, Z., Wakao, S., Fischer, B.B., and Niyogi, K.K. (2009). Sensing and responding to excess light. Annu. Rev. Plant. Biol. 60, 239-260.
  • 6Lichtenthaler, H.K. (2007). Biosynthesis, accumulation and emission of carotenoids, alpha-tocopherol, plastoquinone, and isoprene in leaves under high photosynthetic irradiance. Photosynth. Res. 92, 163-179.
  • 7Lichtenthaler, H.K., Prenzel, U., Douce, R., and Joyard, J. (1981). Localization of prenylquinones in the envelope of spinach chloroplasts. Biochim. Biophys, Acta. 641, 99-105.
  • 8Lichtenthaler, H.K., Schwender, J., Disch, A., and Rohmer, M. (1997). Biosynthesis of isoprenoids in higher plant chloroplasts proceeds via a mevalonate-independent pathway. FEBS Lett. 400, 271-274.
  • 9Lohmann, A., Schottler, M.K., Brehelin, C., Kessler, F., Bock, R., Cahoon, E.B., and Dormann, P. (2006). Deficiency in phylloquinone (vitamin K1) methylation affects prenyl quinone distribution, photosystem Ⅰ abundance, and anthocyanin accumulation in the Arabidopsis AtmenG mutant. J. Biol. Chem. 281, 40461-40472.
  • 10Majeran, W., Zybailov, B., Ytterberg, A.J., Dunsmore, J., Sun, Q., and van Wijk, K.J. (2008). Consequences of C4 differentiation for chloroplast membrane proteomes in maize mesophyll and bundle sheath cells. Mol. Cell. Proteomics. 7, 1609-1638.

共引文献23

同被引文献15

引证文献3

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部