Genetics, Vol. 162, 1979-1993, December 2002, Copyright © 2002

The pam1 Gene Is Required for Meiotic Bouquet Formation and Efficient Homologous Synapsis in Maize (Zea mays L.)

Inna N. Golubovskayaa, Lisa C. Harperb, Wojciech P. Pawlowskib, Denise Schichnesc, and W. Zacheus Candea,b
a Department of Plant and Microbial Biology, University of California, Berkeley, California 94720-3200
b Department of Molecular and Cell Biology, University of California, Berkeley, California 94720-3200
c CNR Biological Imaging, University of California, Berkeley, California 94720-3200

Corresponding author: W. Zacheus Cande, Department of Molecular and Cell Biology, 345 Life Science Addition, Berkeley, CA 94720., zcande{at}uclink4.berkeley.edu (E-mail)

Communicating editor: J. A. BIRCHLER

The clustering of telomeres on the nuclear envelope (NE) during meiotic prophase to form the bouquet arrangement of chromosomes may facilitate homologous chromosome synapsis. The pam1 (plural abnormalities of meiosis 1) gene is the first maize gene that appears to be required for telomere clustering, and homologous synapsis is impaired in pam1. Telomere clustering on the NE is arrested or delayed at an intermediate stage in pam1. Telomeres associate with the NE during the leptotene-zygotene transition but cluster slowly if at all as meiosis proceeds. Intermediate stages in telomere clustering including miniclusters are observed in pam1 but not in wild-type meiocytes. The tight bouquet normally seen at zygotene is a rare event. In contrast, the polarization of centromeres vs. telomeres in the nucleus at the leptotene-zygotene transition is the same in mutant and wild-type cells. Defects in homologous chromosome synapsis include incomplete synapsis, nonhomologous synapsis, and unresolved interlocks. However, the number of RAD51 foci on chromosomes in pam1 is similar to that of wild type. We suggest that the defects in homologous synapsis and the retardation of prophase I arise from the irregularity of telomere clustering and propose that pam1 is involved in the control of bouquet formation and downstream meiotic prophase I events.





This article has been cited by other articles:


Home page
Biophys. JHome page
M. G. L. Gustafsson, L. Shao, P. M. Carlton, C. J. R. Wang, I. N. Golubovskaya, W. Z. Cande, D. A. Agard, and J. W. Sedat
Three-Dimensional Resolution Doubling in Wide-Field Fluorescence Microscopy by Structured Illumination
Biophys. J., June 15, 2008; 94(12): 4957 - 4970.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
S. Smolikov, A. Eizinger, K. Schild-Prufert, A. Hurlburt, K. McDonald, J. Engebrecht, A. M. Villeneuve, and M. P. Colaiacovo
SYP-3 Restricts Synaptonemal Complex Assembly to Bridge Paired Chromosome Axes During Meiosis in Caenorhabditis elegans
Genetics, August 1, 2007; 176(4): 2015 - 2025.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
J. Li, L. C. Harper, I. Golubovskaya, C. R. Wang, D. Weber, R. B. Meeley, J. McElver, B. Bowen, W. Z. Cande, and P. S. Schnable
Functional Analysis of Maize RAD51 in Meiosis and Double-Strand Break Repair
Genetics, July 1, 2007; 176(3): 1469 - 1482.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
X. Yang, L. Timofejeva, H. Ma, and C. A. Makaroff
The Arabidopsis SKP1 homolog ASK1 controls meiotic chromosome remodeling and release of chromatin from the nuclear membrane and nucleolus
J. Cell Sci., September 15, 2006; 119(18): 3754 - 3763.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
I. N. Golubovskaya, O. Hamant, L. Timofejeva, C.-J. R. Wang, D. Braun, R. Meeley, and W. Z. Cande
Alleles of afd1 dissect REC8 functions during meiotic prophase I
J. Cell Sci., August 15, 2006; 119(16): 3306 - 3315.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
H.-Y. Wu and S. M. Burgess
Ndj1, a Telomere-Associated Protein, Promotes Meiotic Recombination in Budding Yeast
Mol. Cell. Biol., May 15, 2006; 26(10): 3683 - 3694.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
C.-J. R. Wang, L. Harper, and W. Z. Cande
High-Resolution Single-Copy Gene Fluorescence in Situ Hybridization and Its Use in the Construction of a Cytogenetic Map of Maize Chromosome 9
PLANT CELL, March 1, 2006; 18(3): 529 - 544.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
E. Martinez-Perez and A. M. Villeneuve
HTP-1-dependent constraints coordinate homolog pairing and synapsis and promote chiasma formation during C. elegans meiosis
Genes & Dev., November 15, 2005; 19(22): 2727 - 2743.
[Abstract] [Full Text] [PDF]


Home page
JCBHome page
E. Trelles-Sticken, C. Adelfalk, J. Loidl, and H. Scherthan
Meiotic telomere clustering requires actin for its formation and cohesin for its resolution
J. Cell Biol., July 18, 2005; 170(2): 213 - 223.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
L. Harper, I. Golubovskaya, and W. Z. Cande
A bouquet of chromosomes
J. Cell Sci., August 15, 2004; 117(18): 4025 - 4032.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
K.-I. Nonomura, M. Nakano, T. Fukuda, M. Eiguchi, A. Miyao, H. Hirochika, and N. Kurata
The Novel Gene HOMOLOGOUS PAIRING ABERRATION IN RICE MEIOSIS1 of Rice Encodes a Putative Coiled-Coil Protein Required for Homologous Chromosome Pairing in Meiosis
PLANT CELL, April 1, 2004; 16(4): 1008 - 1020.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
B. Liebe, M. Alsheimer, C. Hoog, R. Benavente, and H. Scherthan
Telomere Attachment, Meiotic Chromosome Condensation, Pairing, and Bouquet Stage Duration Are Modified in Spermatocytes Lacking Axial Elements
Mol. Biol. Cell, February 1, 2004; 15(2): 827 - 837.
[Abstract] [Full Text] [PDF]


Home page
ScienceHome page
W. P. Pawlowski, I. N. Golubovskaya, L. Timofejeva, R. B. Meeley, W. F. Sheridan, and W. Z. Cande
Coordination of Meiotic Recombination, Pairing, and Synapsis by PHS1
Science, January 2, 2004; 303(5654): 89 - 92.
[Abstract] [Full Text] [PDF]


Home page
Plant CellHome page
W. P. Pawlowski, I. N. Golubovskaya, and W. Z. Cande
Altered Nuclear Distribution of Recombination Protein RAD51 in Maize Mutants Suggests the Involvement of RAD51 in Meiotic Homology Recognition
PLANT CELL, August 1, 2003; 15(8): 1807 - 1816.
[Abstract] [Full Text] [PDF]


Home page
Mol. Biol. CellHome page
P. M. Carlton, C. R. Cowan, and W. Z. Cande
Directed Motion of Telomeres in the Formation of the Meiotic Bouquet Revealed by Time Course and Simulation Analysis
Mol. Biol. Cell, July 1, 2003; 14(7): 2832 - 2843.
[Abstract] [Full Text] [PDF]