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Vol. 11, Issue 11, 3937-3947, November 2000

Essential Roles for Caenorhabditis elegans Lamin Gene in Nuclear Organization, Cell Cycle Progression, and Spatial Organization of Nuclear Pore Complexes

Jun Liu,*dagger Tom Rolef Ben-Shahar,Dagger dagger Dieter Riemer,§ Millet Treinin,|| Perah Spann,Dagger Klaus Weber,§ Andrew Fire,* and Yosef GruenbaumDagger

 *Department of Embryology, Carnegie Institution of Washington, Baltimore, Maryland 21210;  Dagger Department of Genetics, The Life Sciences Institute, The Hebrew University of Jerusalem, Jerusalem 91904, Israel;  §Department of Biochemistry, Max Planck Institute for Biophysical Chemistry, Goettingen D-37077, Germany;  ||Department of Physiology, Hadassah Medical School, The Hebrew University of Jerusalem, Jerusalem 91120, Israel.

Caenorhabditis elegans has a single lamin gene, designated lmn-1 (previously termed CeLam-1). Antibodies raised against the lmn-1 product (Ce-lamin) detected a 64-kDa nuclear envelope protein. Ce-lamin was detected in the nuclear periphery of all cells except sperm and was found in the nuclear interior in embryonic cells and in a fraction of adult cells. Reductions in the amount of Ce-lamin protein produce embryonic lethality. Although the majority of affected embryos survive to produce several hundred nuclei, defects can be detected as early as the first nuclear divisions. Abnormalities include rapid changes in nuclear morphology during interphase, loss of chromosomes, unequal separation of chromosomes into daughter nuclei, abnormal condensation of chromatin, an increase in DNA content, and abnormal distribution of nuclear pore complexes (NPCs). Under conditions of incomplete RNA interference, a fraction of embryos escaped embryonic arrest and continue to develop through larval life. These animals exhibit additional phenotypes including sterility and defective segregation of chromosomes in germ cells. Our observations show that lmn-1 is an essential gene in C. elegans, and that the nuclear lamins are involved in chromatin organization, cell cycle progression, chromosome segregation, and correct spacing of NPCs.


dagger These authors contributed equally to the work described in this manuscript.

Corresponding author. E-mail address: gru{at}vms.huji.ac.il


Molecular Biology of the Cell
Vol. 11, 3937-3947, November 2000
Copyright © 2000 by The American Society for Cell Biology



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