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024 7 |a 10.1016/j.plaphy.2013.05.029  |2 doi 
028 5 2 |a pubmed25n0761.xml 
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041 |a eng 
100 1 |a Pietrowska-Borek, Małgorzata  |e verfasserin  |4 aut 
245 1 0 |a Both cyclic-AMP and cyclic-GMP can act as regulators of the phenylpropanoid pathway in Arabidopsis thaliana seedlings 
264 1 |c 2013 
336 |a Text  |b txt  |2 rdacontent 
337 |a ƒaComputermedien  |b c  |2 rdamedia 
338 |a ƒa Online-Ressource  |b cr  |2 rdacarrier 
500 |a Date Completed 13.02.2014 
500 |a Date Revised 30.09.2020 
500 |a published: Print-Electronic 
500 |a Citation Status MEDLINE 
520 |a Copyright © 2013 Elsevier Masson SAS. All rights reserved. 
520 |a Cyclic nucleotides (cAMP and cGMP) are important signaling molecules that control a range of cellular functions and modulate different reactions. It is known that under abiotic or biotic stress plant cells synthesize these nucleotides and that they also enhance the activity of the phenylpropanoid pathway. Wondering what is the relation between these two facts, we investigated how the exogenously applied membrane-permeable derivatives, 8-Br-cAMP or 8-Br-cGMP, which are believed to act as the original cyclic nucleotides, affect the expression of the genes for and the specific activity of three enzymes of the phenylpropanoid pathway in Arabidopsis thaliana seedlings. We found that the expression of the genes of phenylalanine ammonia-lyase (PAL2), 4-coumarate:coenzyme A ligase (4CL1) and chalcone synthase (CHS), and the specific activities of PAL (EC 4.3.1.5), 4CL (EC 6.2.1.12) and CHS (EC 2.3.1.74) were induced in the same way by either of these cyclic nucleotides used at 5 μM concentration. None of the possible cAMP and cGMP degradation products (AMP, GMP, adenosine or guanosine) evoked such effects. Expression of PAL1, 4CL2 and 4CL3 were practically not affected. Although the investigated nucleotides induced rapid expression of the aforementioned enzymes, they did not affect the level of anthocyanins within the same period. We discuss the effects exerted by the exogenously administered cyclic nucleotides, their relation with stress and the role which the phenylpropanoid pathways the cyclic nucleotides may play in plants 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a 4-Coumarate:coenzyme A ligase 
650 4 |a 4-coumarate:coenzyme A ligase 
650 4 |a 4CL 
650 4 |a Adenosine 3′,5′-cyclic monophosphate 
650 4 |a Arabidopsis thaliana 
650 4 |a CH 
650 4 |a Chalcone synthase 
650 4 |a Guanosine 3′,5′-cyclic monophosphate 
650 4 |a PAL 
650 4 |a Phenylalanine ammonia-lyase 
650 4 |a adenosine 3′,5′-cyclic monophosphate 
650 4 |a cAMP 
650 4 |a cGMP 
650 4 |a cNMP 
650 4 |a chalcone synthase 
650 4 |a guanosine 3′,5′-cyclic monophosphate 
650 4 |a nucleoside 3′,5′-cyclic monophosphate 
650 4 |a phenylalanine ammonia-lyase 
650 7 |a Anthocyanins  |2 NLM 
650 7 |a Arabidopsis Proteins  |2 NLM 
650 7 |a Phenols  |2 NLM 
650 7 |a 8-bromocyclic GMP  |2 NLM 
650 7 |a 31356-94-2  |2 NLM 
650 7 |a Cyclic AMP  |2 NLM 
650 7 |a E0399OZS9N  |2 NLM 
650 7 |a Acyltransferases  |2 NLM 
650 7 |a EC 2.3.-  |2 NLM 
650 7 |a flavanone synthetase  |2 NLM 
650 7 |a EC 2.3.1.74  |2 NLM 
650 7 |a Phenylalanine Ammonia-Lyase  |2 NLM 
650 7 |a EC 4.3.1.24  |2 NLM 
650 7 |a Coenzyme A Ligases  |2 NLM 
650 7 |a EC 6.2.1.-  |2 NLM 
650 7 |a Cyclic GMP  |2 NLM 
650 7 |a H2D2X058MU  |2 NLM 
700 1 |a Nuc, Katarzyna  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Plant physiology and biochemistry : PPB  |d 1991  |g 70(2013) vom: 10. Sept., Seite 142-9  |w (DE-627)NLM098178261  |x 1873-2690  |7 nnns 
773 1 8 |g volume:70  |g year:2013  |g day:10  |g month:09  |g pages:142-9 
856 4 0 |u http://dx.doi.org/10.1016/j.plaphy.2013.05.029  |3 Volltext 
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952 |d 70  |j 2013  |b 10  |c 09  |h 142-9