001     49905
005     20180211183847.0
024 7 _ |2 pmid
|a pmid:16333638
024 7 _ |2 DOI
|a 10.1007/s00425-005-0181-0
024 7 _ |2 WOS
|a WOS:000237335300020
037 _ _ |a PreJuSER-49905
041 _ _ |a eng
082 _ _ |a 580
084 _ _ |2 WoS
|a Plant Sciences
100 1 _ |a Matsubara, S.
|b 0
|u FZJ
|0 P:(DE-Juel1)129358
245 _ _ |a Nocturnal changes in leaf growth of Populus deltoides are controlled by cytoplasmic growth
260 _ _ |a Berlin
|b Springer
|c 2006
300 _ _ |a 1315 - 1328
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|0 0
|2 EndNote
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |a Planta
|x 0032-0935
|0 4992
|y 6
|v 223
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a Growing leaves do not expand at a constant rate but exhibit pronounced diel growth rhythms. However, the mechanisms giving rise to distinct diel growth dynamics in different species are still largely unknown. As a first step towards identifying genes controlling rate and timing of leaf growth, we analysed the transcriptomes of rapidly expanding and fully expanded leaves of Populus deltoides Bartr. ex. Marsh at points of high and low expansion at night. Tissues with well defined temporal growth rates were harvested using an online growth-monitoring system based on a digital image sequence processing method developed for quantitative mapping of dicot leaf growth. Unlike plants studied previously, leaf growth in P. deltoides was characterised by lack of a base-tip gradient across the lamina, and by maximal and minimal growth at dusk and dawn, respectively. Microarray analysis revealed that the nocturnal decline in growth coincided with a concerted down-regulation of ribosomal protein genes, indicating deceleration of cytoplasmic growth. In a subsequent time-course experiment, Northern blotting and real-time RT-PCR confirmed that the ribosomal protein gene RPL12 and a cell-cycle gene H2B were down-regulated after midnight following a decrease in cellular carbohydrate concentrations. Thus, we propose that the spatio-temporal growth pattern in leaves of P. deltoides primarily arises from cytoplasmic growth whose activity increases from afternoon to midnight and thereafter decreases in this species.
536 _ _ |a Terrestrische Umwelt
|c P24
|2 G:(DE-HGF)
|0 G:(DE-Juel1)FUEK407
|x 0
588 _ _ |a Dataset connected to Web of Science, Pubmed
650 _ 2 |2 MeSH
|a Carbohydrate Metabolism
650 _ 2 |2 MeSH
|a Circadian Rhythm
650 _ 2 |2 MeSH
|a Cluster Analysis
650 _ 2 |2 MeSH
|a Cytoplasm: physiology
650 _ 2 |2 MeSH
|a Darkness
650 _ 2 |2 MeSH
|a Gene Expression Profiling
650 _ 2 |2 MeSH
|a Gene Expression Regulation, Plant
650 _ 2 |2 MeSH
|a Genes, Plant
650 _ 2 |2 MeSH
|a Histones: genetics
650 _ 2 |2 MeSH
|a Histones: metabolism
650 _ 2 |2 MeSH
|a Oligonucleotide Array Sequence Analysis
650 _ 2 |2 MeSH
|a Plant Leaves: cytology
650 _ 2 |2 MeSH
|a Plant Leaves: growth & development
650 _ 2 |2 MeSH
|a Plant Proteins: genetics
650 _ 2 |2 MeSH
|a Plant Proteins: metabolism
650 _ 2 |2 MeSH
|a Populus: cytology
650 _ 2 |2 MeSH
|a Populus: growth & development
650 _ 2 |2 MeSH
|a Ribosomal Proteins: genetics
650 _ 2 |2 MeSH
|a Ribosomal Proteins: metabolism
650 _ 7 |0 0
|2 NLM Chemicals
|a Histones
650 _ 7 |0 0
|2 NLM Chemicals
|a Plant Proteins
650 _ 7 |0 0
|2 NLM Chemicals
|a Ribosomal Proteins
650 _ 7 |a J
|2 WoSType
653 2 0 |2 Author
|a cell cycle
653 2 0 |2 Author
|a cytoplasmic growth
653 2 0 |2 Author
|a leaf growth
653 2 0 |2 Author
|a microarray
653 2 0 |2 Author
|a Populus
653 2 0 |2 Author
|a ribosomal protein
700 1 _ |a Hurry, V.
|b 1
|0 P:(DE-HGF)0
700 1 _ |a Druart, N.
|b 2
|0 P:(DE-HGF)0
700 1 _ |a Benedict, C.
|b 3
|0 P:(DE-HGF)0
700 1 _ |a Janzik, I.
|b 4
|u FZJ
|0 P:(DE-Juel1)129338
700 1 _ |a Chavarria-Krauser, A.
|b 5
|u FZJ
|0 P:(DE-Juel1)VDB33618
700 1 _ |a Walter, A.
|b 6
|u FZJ
|0 P:(DE-Juel1)VDB2595
700 1 _ |a Schurr, U.
|b 7
|u FZJ
|0 P:(DE-Juel1)129402
773 _ _ |a 10.1007/s00425-005-0181-0
|g Vol. 223, p. 1315 - 1328
|p 1315 - 1328
|q 223<1315 - 1328
|0 PERI:(DE-600)1463030-8
|t Planta
|v 223
|y 2006
|x 0032-0935
856 7 _ |u http://dx.doi.org/10.1007/s00425-005-0181-0
909 C O |o oai:juser.fz-juelich.de:49905
|p VDB
913 1 _ |k P24
|v Terrestrische Umwelt
|l Terrestrische Umwelt
|b Erde und Umwelt
|0 G:(DE-Juel1)FUEK407
|x 0
914 1 _ |y 2006
915 _ _ |0 StatID:(DE-HGF)0010
|a JCR/ISI refereed
920 1 _ |d 31.12.2006
|g ICG
|k ICG-III
|l Phytosphäre
|0 I:(DE-Juel1)VDB49
|x 0
920 1 _ |0 I:(DE-82)080011_20140620
|k JARA-ENERGY
|l Jülich-Aachen Research Alliance - Energy
|g JARA
|x 1
970 _ _ |a VDB:(DE-Juel1)78046
980 _ _ |a VDB
980 _ _ |a ConvertedRecord
980 _ _ |a journal
980 _ _ |a I:(DE-Juel1)IBG-2-20101118
980 _ _ |a I:(DE-82)080011_20140620
980 _ _ |a UNRESTRICTED
981 _ _ |a I:(DE-Juel1)IBG-2-20101118
981 _ _ |a I:(DE-Juel1)VDB1047


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