2016
DOI: 10.1105/tpc.15.01003
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Histone H3 Dynamics Reveal Domains with Distinct Proliferation Potential in the Arabidopsis Root

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Cited by 77 publications
(102 citation statements)
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“…Furthermore, ongoing DNA synthesis in cotyledons has been shown by incorporation in of the nucleotide analog 5‐ethynyl‐2′‐deoxyuridine (EdU) 7‐d‐old seedlings (Jiang & Berger, ), together suggesting that DNA‐synthesis‐dependent deposition can explain the observed increased H3.1 occupancy at repetitive sequences at 5 dag. To explain the increase in H3.1 occupancy specifically at heterochromatin, we can envisage that after a genome‐wide incorporation during S‐phase, H3.1 is exchanged to H3.3 either in a transcription‐dependent manner at the genic regions analyzed here or globally in euchromatin as described previously during the transition from cell proliferation to differentiation in the root (Otero et al ., ). Interestingly, most H3.1‐encoding genes are not expressed in the dry seed (Kawakatsu et al ., ; Narsai et al ., ), in agreement with absence of replicative activity (Barroco et al ., ) pointing towards a peculiar H3.1 : H3.3 balance in the dry seed that might favor chromatin decondensation during germination.…”
Section: Discussionmentioning
confidence: 97%
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“…Furthermore, ongoing DNA synthesis in cotyledons has been shown by incorporation in of the nucleotide analog 5‐ethynyl‐2′‐deoxyuridine (EdU) 7‐d‐old seedlings (Jiang & Berger, ), together suggesting that DNA‐synthesis‐dependent deposition can explain the observed increased H3.1 occupancy at repetitive sequences at 5 dag. To explain the increase in H3.1 occupancy specifically at heterochromatin, we can envisage that after a genome‐wide incorporation during S‐phase, H3.1 is exchanged to H3.3 either in a transcription‐dependent manner at the genic regions analyzed here or globally in euchromatin as described previously during the transition from cell proliferation to differentiation in the root (Otero et al ., ). Interestingly, most H3.1‐encoding genes are not expressed in the dry seed (Kawakatsu et al ., ; Narsai et al ., ), in agreement with absence of replicative activity (Barroco et al ., ) pointing towards a peculiar H3.1 : H3.3 balance in the dry seed that might favor chromatin decondensation during germination.…”
Section: Discussionmentioning
confidence: 97%
“…Chromatin assembly mediated by CAF-1 is required for CC formation H3.1 is deposited by the CAF-1 complex that operates in a DNA-synthesis dependent manner (Otero et al, 2016;Jiang & Berger, 2017), whereas the HIR complex is responsible for assembly of the replacement variant H3.3 Duc et al, 2015). FASCIATA 1 (FAS1), FASCIATA 2 (FAS2) and HISTONE REGULATOR A (HIRA), encoding two subunits of the Arabidopsis CAF-1 complex, and the central subunit of the HIR complex, respectively, are expressed during early postgermination development in cotyledons (Fig.…”
Section: H31 Occupancy Increases At Repetitive Sequences During CC Fmentioning
confidence: 99%
“…We used live imaging to study CDT1a dynamics during the cell cycle in the growing Arabidopsis root meristem cells by following the CDT1a-CFP signal in plants also expressing the constitutively expressed HTR5 histone H3.3-mRFP (Otero et al, 2016). Since mitotic cells did not contain CDT1a-CFP we started to follow the progression of mitotic cells into the next cell cycle.…”
Section: Cdt1a Protein Is Loaded In Early G1 and Degraded At The G1/smentioning
confidence: 99%
“…Nuestro grupo ha estudiado la dinámica de incorporación de histona H3 durante el desarrollo de órganos [6] y ha podido identificar una población celular única que se encuentra desarrollando su último ciclo celular antes de iniciar la diferenciación [7].…”
Section: Summary Organogenesis Requires a Strict Coordination Betweenunclassified