Ciencias,UNAM

Firing of transcription and compartmentalization of splicing factors in tomato radicle nuclei during germination

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dc.contributor.author Moreno-Díaz de la Espina, S
dc.contributor.author Juárez-Chavero, S
dc.contributor.author Echeverria-Martínez, OM
dc.contributor.author Vázquez-Nin, Gerardo Hebert
dc.date.accessioned 2011-01-22T10:27:09Z
dc.date.available 2011-01-22T10:27:09Z
dc.date.issued 2007
dc.identifier.issn 2484900
dc.identifier.uri http://hdl.handle.net/11154/1113
dc.description.abstract Background information. Germination is a well-characterized process in which embryo cells of seeds experience a programmed transition from quiescence to proliferation. For this reason they constitute a very good system to analyse nuclear evolution from a dehydrated practically inactive state until the steady state of proliferation. We analysed the temporal and spatial organization of transcription and splicing factors in nuclei of tomato radicle cells during germination. To address this issue we performed in situ immunodetection of several markers of these processes: the Z-DNA stretches forming behind the active RNA polymerases, the splicing proteins U2B" and Sm, and the trimethyl guanosin cap of small nuclear RNA. The concomitant structural changes of the different nuclear compartments were studied in meristematic nuclei by electron microscopy and high-resolution cytochemistry for DNA and ribonucleoproteins. Results. In quiescent cells practically no Z-DNA stretches were detected and splicing components localized mainly to one or two Cajal bodies associated to the nucleolus. In early germination, a massive de-condensation of chromatin and nucleolar Z-DNA conformation stretches were first detected, followed by the relocation of scarce splicing components to the small interchromatin spaces. Nucleoplasmic Z-DNA stretches were not detected until 4 h of imbibition and were accompanied by an important increase of splicing components in this nuclear domain. Soon after the post-germination stage, transcription and splicing topology and nuclear organization in meristematic nuclei resemble those in steady state growing tomato roots. Conclusions. Our results demonstrate that, in tomato, dormant nuclei splicing factors are stored in nucleolar Cajal bodies. In early germination, RNA polymerase I transcription is first activated, whereas mRNA transcription is fired later and is accompanied by a massive de-condensation of chromatin and accumulation of splicing factors in the interchromatin domains. Nucleoplasmic Cajal bodies appear later in germination. en_US
dc.language.iso en en_US
dc.title Firing of transcription and compartmentalization of splicing factors in tomato radicle nuclei during germination
dc.type Artículo de investigación en_US
dc.type Inglés
dc.identifier.idprometeo 1112
dc.identifier.doi 10.1042/BC20070026
dc.source.novolpages 99(9):519-530
dc.subject.wos Cell Biology
dc.description.index WoS: SCI, SSCI o AHCI
dc.subject.keywords germination
dc.subject.keywords nuclear organization
dc.subject.keywords splicing factors
dc.subject.keywords tomato
dc.subject.keywords Z-DNA
dc.relation.journal Biology of the Cell
dc.description.Departamento Departamento de Biología Comparada

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