spacer gif spacer gif spacer gif spacer gif Propose a workshop for 2011 spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wiekowski, M.
Right arrow Articles by DePamphilis, M. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wiekowski, M.
Right arrow Articles by DePamphilis, M. L.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Journal of Cell Science, Vol 110, Issue 10 1147-1158, Copyright © 1997 by Company of Biologists


JOURNAL ARTICLES

Changes in histone synthesis and modification at the beginning of mouse development correlate with the establishment of chromatin mediated repression of transcription

M Wiekowski, M Miranda, JY Nothias and ML DePamphilis
Roche Institute of Molecular Biology, Roche Research Center, Nutley, NJ 07110, USA.

The transition from a late 1-cell mouse embryo to a 4-cell embryo, the period when zygotic gene expression begins, is accompanied by an increasing ability to repress the activities of promoters and replication origins. Since this repression can be relieved by either butyrate or enhancers, it appears to be mediated through chromatin structure. Here we identify changes in the synthesis and modification of chromatin bound histones that are consistent with this hypothesis. Oocytes, which can repress promoter activity, synthesized a full complement of histones, and histone synthesis up to the early 2-cell stage originated from mRNA inherited from the oocyte. However, while histones H3 and H4 continued to be synthesized in early 1-cell embryos, synthesis of histones H2A, H2B and H1 (proteins required for chromatin condensation) was delayed until the late 1-cell stage, reaching their maximum rate in early 2-cell embryos. Moreover, histone H4 in both 1-cell and 2-cell embryos was predominantly diacetylated (a modification that facilitates transcription). Deacetylation towards the unacetylated and monoacetylated H4 population in fibroblasts began at the late 2-cell to 4-cell stage. Arresting development at the beginning of S-phase in 1-cell embryos prevented both the appearance of chromatin-mediated repression of transcription in paternal pronuclei and synthesis of new histones. These changes correlated with the establishment of chromatin-mediated repression during formation of a 2-cell embryo, and the increase in repression from the 2-cell to 4-cell stage as linker histone H1 accumulates and core histones are deacetylated.
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
ReproductionHome page
L. Magnani and R. A Cabot
Manipulation of SMARCA2 and SMARCA4 transcript levels in porcine embryos differentially alters development and expression of SMARCA1, SOX2, NANOG, and EIF1
Reproduction, January 1, 2009; 137(1): 23 - 33.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
T. Thomas, M. P. Dixon, A. J. Kueh, and A. K. Voss
Mof (MYST1 or KAT8) Is Essential for Progression of Embryonic Development Past the Blastocyst Stage and Required for Normal Chromatin Architecture
Mol. Cell. Biol., August 15, 2008; 28(16): 5093 - 5105.
[Abstract] [Full Text] [PDF]


Home page
ReproductionHome page
M. M Seneda, M. Godmann, B. D Murphy, S. Kimmins, and V. Bordignon
Developmental regulation of histone H3 methylation at lysine 4 in the porcine ovary
Reproduction, June 1, 2008; 135(6): 829 - 838.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
A. Rybouchkin, Y. Kato, and Y. Tsunoda
Role of Histone Acetylation in Reprogramming of Somatic Nuclei Following Nuclear Transfer
Biol Reprod, June 1, 2006; 74(6): 1083 - 1089.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
N. Mano, K. Kasuga, N. Kobayashi, and J. Goto
A Nonenzymatic Modification of the Amino-terminal Domain of Histone H3 by Bile Acid Acyl Adenylate
J. Biol. Chem., December 31, 2004; 279(53): 55034 - 55041.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
M. T. Fiorenza, A. Bevilacqua, S. Canterini, S. Torcia, M. Pontecorvi, and F. Mangia
Early Transcriptional Activation of the Hsp70.1 Gene by Osmotic Stress in One-Cell Embryos of the Mouse
Biol Reprod, June 1, 2004; 70(6): 1606 - 1613.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
G. Fu, P. Ghadam, A. Sirotkin, S. Khochbin, A. I. Skoultchi, and H. J. Clarke
Mouse Oocytes and Early Embryos Express Multiple Histone H1 Subtypes
Biol Reprod, May 1, 2003; 68(5): 1569 - 1576.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
S. McGraw, C. Robert, L. Massicotte, and M.-A. Sirard
Quantification of Histone Acetyltransferase and Histone Deacetylase Transcripts During Early Bovine Embryo Development
Biol Reprod, February 1, 2003; 68(2): 383 - 389.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
J.-M. Kim, A. Ogura, M. Nagata, and F. Aoki
Analysis of the Mechanism for Chromatin Remodeling in Embryos Reconstructed by Somatic Nuclear Transfer
Biol Reprod, September 1, 2002; 67(3): 760 - 766.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
M. I. Aladjem, L. W. Rodewald, C. M. Lin, S. Bowman, D. M. Cimbora, L. L. Brody, E. M. Epner, M. Groudine, and G. M. Wahl
Replication Initiation Patterns in the {beta}-Globin Loci of Totipotent and Differentiated Murine Cells: Evidence for Multiple Initiation Regions
Mol. Cell. Biol., January 15, 2002; 22(2): 442 - 452.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
P. Allard, M. J. Champigny, S. Skoggard, J. A. Erkmann, M. L. Whitfield, W. F. Marzluff, and H. J. Clarke
Stem-loop binding protein accumulates during oocyte maturation and is not cell-cycle-regulated in the early mouse embryo
J. Cell Sci., January 12, 2002; 115(23): 4577 - 4586.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
L. Rastelli, K. Robinson, Y. Xu, and S. Majumder
Reconstitution of Enhancer Function in Paternal Pronuclei of One-Cell Mouse Embryos
Mol. Cell. Biol., August 15, 2001; 21(16): 5531 - 5540.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
J. Ma, P. Svoboda, R. M. Schultz, and P. Stein
Regulation of Zygotic Gene Activation in the Preimplantation Mouse Embryo: Global Activation and Repression of Gene Expression
Biol Reprod, June 1, 2001; 64(6): 1713 - 1721.
[Abstract] [Full Text]


Home page
DevelopmentHome page
M Tanaka, J. Hennebold, J Macfarlane, and E. Adashi
A mammalian oocyte-specific linker histone gene H1oo: homology with the genes for the oocyte-specific cleavage stage histone (cs-H1) of sea urchin and the B4/H1M histone of the frog
Development, January 3, 2001; 128(5): 655 - 664.
[Abstract] [PDF]


Home page
Genes Dev.Home page
J. Zhao, B. K. Kennedy, B. D. Lawrence, D. A. Barbie, A. G. Matera, J. A. Fletcher, and E. Harlow
NPAT links cyclin E-Cdk2 to the regulation of replication-dependent histone gene transcription
Genes & Dev., September 15, 2000; 14(18): 2283 - 2297.
[Abstract] [Full Text]


Home page
J. Cell Sci.Home page
P. Adenot, E Campion, E Legouy, C. Allis, S Dimitrov, J Renard, and E. Thompson
Somatic linker histone H1 is present throughout mouse embryogenesis and is not replaced by variant H1 degrees
J. Cell Sci., January 8, 2000; 113(16): 2897 - 2907.
[Abstract] [PDF]


Home page
DevelopmentHome page
A Bevilacqua, M. Fiorenza, and F Mangia
A developmentally regulated GAGA box-binding factor and Sp1 are required for transcription of the hsp70.1 gene at the onset of mouse zygotic genome activation
Development, January 4, 2000; 127(7): 1541 - 1551.
[Abstract] [PDF]


Home page
Biol. Reprod.Home page
E. Memili and N. L. First
Control of Gene Expression at the Onset of Bovine Embryonic Development
Biol Reprod, November 1, 1999; 61(5): 1198 - 1207.
[Abstract] [Full Text]


Home page
Mol Hum ReprodHome page
R.G. Edwards and H. K. Beard
Hypothesis: sex determination and germline formation are committed at the pronucleate stage in mammalian embryos
Mol. Hum. Reprod., July 1, 1999; 5(7): 595 - 606.
[Full Text] [PDF]


Home page
Biol. Reprod.Home page
V. Bordignon, H. J. Clarke, and L. C. Smith
Developmentally Regulated Loss and Reappearance of Immunoreactive Somatic Histone H1 on Chromatin of Bovine Morula-Stage Nuclei Following Transplantation into Oocytes
Biol Reprod, July 1, 1999; 61(1): 22 - 30.
[Abstract] [Full Text]


Home page
Biol. Reprod.Home page
P. A. De Sousa,, A. J. Watson,, and R. M. Schultz
Transient Expression of a Translation Initiation Factor Is Conservatively Associated with Embryonic Gene Activation in Murine and Bovine Embryos
Biol Reprod, October 1, 1998; 59(4): 969 - 977.
[Abstract] [Full Text]




© The Company of Biologists Ltd 1997