spacer gif spacer gif spacer gif spacer gif 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 Huynh, J.
Right arrow Articles by St Johnston, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Huynh, J.
Right arrow Articles by St Johnston, D.
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?

Development, Vol 127, Issue 13 2785-2794, Copyright © 2000 by Company of Biologists


JOURNAL ARTICLES

The role of BicD, egl, orb and the microtubules in the restriction of meiosis to the Drosophila oocyte

J Huynh and D St Johnston
The Wellcome/CRC Institute and the Department of Genetics, University of Cambridge, Tennis Court Rd, Cambridge, CB2 1QR, UK.

The oocyte is the only cell in Drosophila that goes through meiosis with meiotic recombination, but several germ cells in a 16-cell cyst enter meiosis and form synaptonemal complexes (SC) before one cell is selected to become the oocyte. Using an antibody that recognises a component of the SC or the synapsed chromosomes, we have analysed how meiosis becomes restricted to one cell, in relation to the other events in oocyte determination. Although BicD and egl mutants both cause the development of cysts with no oocyte, they have opposite effects on the behaviour of the SC: none of the cells in the cyst form SC in BicD null mutants, whereas all of the cells do in egl and orb mutants. Furthermore, unlike all cytoplasmic markers for the oocyte, the SC still becomes restricted to one cell when the microtubules are depolymerised, even though the BicD/Egl complex is not localised. These results lead us to propose a model in which BicD, Egl and Orb control entry into meiosis by regulating translation.
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
Cold Spring Harb. Perspect. Biol.Home page
S. Roth and J. A. Lynch
Symmetry Breaking During Drosophila Oogenesis
Cold Spring Harb Perspect Biol, August 1, 2009; 1(2): a001891 - a001891.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
K. Narbonne-Reveau and M. Lilly
The Cyclin-dependent Kinase Inhibitor Dacapo Promotes Genomic Stability during Premeiotic S Phase
Mol. Biol. Cell, April 1, 2009; 20(7): 1960 - 1969.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
E. F. Joyce and K. S. McKim
Drosophila PCH2 Is Required for a Pachytene Checkpoint That Monitors Double-Strand-Break-Independent Events Leading to Meiotic Crossover Formation
Genetics, January 1, 2009; 181(1): 39 - 51.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
J. P. Blumenstiel, R. Fu, W. E. Theurkauf, and R. S. Hawley
Components of the RNAi Machinery That Mediate Long-Distance Chromosomal Associations Are Dispensable for Meiotic and Early Somatic Homolog Pairing in Drosophila melanogaster
Genetics, November 1, 2008; 180(3): 1355 - 1365.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
P. Benoit, C. Papin, J. E. Kwak, M. Wickens, and M. Simonelig
PAP- and GLD-2-type poly(A) polymerases are required sequentially in cytoplasmic polyadenylation and oogenesis in Drosophila
Development, June 1, 2008; 135(11): 1969 - 1979.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
V. Barbosa, N. Kimm, and R. Lehmann
A Maternal Screen for Genes Regulating Drosophila Oocyte Polarity Uncovers New Steps in Meiotic Progression
Genetics, August 1, 2007; 176(4): 1967 - 1977.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
J. Kimble and D. C. Page
The Mysteries of Sexual Identity: The Germ Cell's Perspective
Science, April 20, 2007; 316(5823): 400 - 401.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
J.-B. Coutelis and A. Ephrussi
Rab6 mediates membrane organization and determinant localization during Drosophila oogenesis
Development, April 1, 2007; 134(7): 1419 - 1430.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
K. Roper
Rtnl1 is enriched in a specialized germline ER that associates with ribonucleoprotein granule components
J. Cell Sci., March 15, 2007; 120(6): 1081 - 1092.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
R. McCaffrey, D. St Johnston, and A. Gonzalez-Reyes
Drosophila mus301/spindle-C Encodes a Helicase With an Essential Role in Double-Strand DNA Break Repair and Meiotic Progression
Genetics, November 1, 2006; 174(3): 1273 - 1285.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
V. Mirouse, E. Formstecher, and J.-L. Couderc
Interaction between Polo and BicD proteins links oocyte determination and meiosis control in Drosophila
Development, October 15, 2006; 133(20): 4005 - 4013.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
B. E. Thompson, D. S. Bernstein, J. L. Bachorik, A. G. Petcherski, M. Wickens, and J. Kimble
Dose-dependent control of proliferation and sperm specification by FOG-1/CPEB
Development, August 1, 2005; 132(15): 3471 - 3481.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
T. Iida and M. A. Lilly
missing oocyte encodes a highly conserved nuclear protein required for the maintenance of the meiotic cycle and oocyte identity in Drosophila
Development, March 1, 2004; 131(5): 1029 - 1039.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
U. Abdu, A. Gonzalez-Reyes, A. Ghabrial, and T. Schupbach
The Drosophila spn-D Gene Encodes a RAD51C-Like Protein That Is Required Exclusively During Meiosis
Genetics, September 1, 2003; 165(1): 197 - 204.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
J. Z. Morris, C. Navarro, and R. Lehmann
Identification and Analysis of Mutations in bob, Doa and Eight New Genes Required for Oocyte Specification and Development in Drosophila melanogaster
Genetics, August 1, 2003; 164(4): 1435 - 1446.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
A. Hong, S. Lee-Kong, T. Iida, I. Sugimura, and M. A. Lilly
The p27cip/kip ortholog dacapo maintains the Drosophila oocyte in prophase of meiosis I
Development, April 1, 2003; 130(7): 1235 - 1242.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
S. D. Findley, M. Tamanaha, N. J. Clegg, and H. Ruohola-Baker
Maelstrom, a Drosophila spindle-class gene, encodes a protein that colocalizes with Vasa and RDE1/AGO1 homolog, Aubergine, in nuage
Development, March 1, 2003; 130(5): 859 - 871.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
E. Mathe, Y. H. Inoue, W. Palframan, G. Brown, and D. M. Glover
Orbit/Mast, the CLASP orthologue of Drosophila, is required for asymmetric stem cell and cystocyte divisions and development of the polarised microtubule network that interconnects oocyte and nurse cells during oogenesis
Development, March 1, 2003; 130(5): 901 - 915.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
G. Minestrini, E. Mathe, and D. M. Glover
Domains of the Pavarotti kinesin-like protein that direct its subcellular distribution: effects of mislocalisation on the tubulin and actin cytoskeleton during Drosophila oogenesis
J. Cell Sci., February 15, 2002; 115(4): 725 - 736.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
S. Doronkin, I. Djagaeva, and S. K. Beckendorf
CSN5/Jab1 mutations affect axis formation in the Drosophila oocyte by activating a meiotic checkpoint
Development, January 11, 2002; 129(21): 5053 - 5064.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
D. N. Cox, S. A. Seyfried, L. Y. Jan, and Y. N. Jan
Bazooka and atypical protein kinase C are required to regulate oocyte differentiation in the Drosophila ovary
PNAS, December 4, 2001; 98(25): 14475 - 14480.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
S. L. Page and R. S. Hawley
c(3)G encodes a Drosophila synaptonemal complex protein
Genes & Dev., December 1, 2001; 15(23): 3130 - 3143.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
J Bolvar, J. Huynh, H Lpez-Schier, C Gonzlez, D St Johnston, and A Gonzlez-Reyes
Centrosome migration into the Drosophila oocyte is independent of BicD and egl, and of the organisation of the microtubule cytoskeleton
Development, January 5, 2001; 128(10): 1889 - 1897.
[Abstract] [PDF]


Home page
DevelopmentHome page
J. Huynh, J. Shulman, R Benton, and D St Johnston
PAR-1 is required for the maintenance of oocyte fate in Drosophila
Development, January 4, 2001; 128(7): 1201 - 1209.
[Abstract] [PDF]


Home page
Genes Dev.Home page
C. Luitjens, M. Gallegos, B. Kraemer, J. Kimble, and M. Wickens
CPEB proteins control two key steps in spermatogenesis in C. elegans
Genes & Dev., October 15, 2000; 14(20): 2596 - 2609.
[Abstract] [Full Text]


Home page
Mol. Biol. CellHome page
E. A. Manheim, J. K. Jang, D. Dominic, and K. S. McKim
Cytoplasmic Localization and Evolutionary Conservation of MEI-218, a Protein Required for Meiotic Crossing-over in Drosophila
Mol. Biol. Cell, January 1, 2002; 13(1): 84 - 95.
[Abstract] [Full Text] [PDF]




© The Company of Biologists Ltd 2000