» Articles » PMID: 17967950

Microtubules Are Involved in Anterior-posterior Axis Formation in C. Elegans Embryos

Overview
Journal J Cell Biol
Specialty Cell Biology
Date 2007 Oct 31
PMID 17967950
Citations 36
Authors
Affiliations
Soon will be listed here.
Abstract

Microtubules deliver positional signals and are required for establishing polarity in many different organisms and cell types. In Caenorhabditis elegans embryos, posterior polarity is induced by an unknown centrosome-dependent signal. Whether microtubules are involved in this signaling process has been the subject of controversy. Although early studies supported such an involvement (O'Connell, K.F., K.N. Maxwell, and J.G. White. 2000. Dev. Biol. 222:55-70; Wallenfang, M.R., and G. Seydoux. 2000. Nature. 408:89-92; Hamill, D.R., A.F. Severson, J.C. Carter, and B. Bowerman. 2002. Dev. Cell. 3:673-684), recent work involving RNA interference knockdown of tubulin led to the conclusion that centrosomes induce polarity independently of microtubules (Cowan, C.R., and A.A. Hyman. 2004. Nature. 431:92-96; Sonneville, R., and P. Gonczy. 2004. Development. 131: 3527-3543). In this study, we investigate the consequences of tubulin knockdown on polarity signaling. We find that tubulin depletion delays polarity induction relative to wild type and that polarity only occurs when a small, late-growing microtubule aster is visible at the centrosome. We also show that the process of a normal meiosis produces a microtubule-dependent polarity signal and that the relative levels of anterior and posterior PAR (partitioning defective) polarity proteins influence the response to polarity signaling. Our results support a role for microtubules in the induction of embryonic polarity in C. elegans.

Citing Articles

Quantitative perturbation-phenotype maps reveal nonlinear responses underlying robustness of PAR-dependent asymmetric cell division.

Rodrigues N, Bland T, Ng K, Hirani N, Goehring N PLoS Biol. 2024; 22(12):e3002437.

PMID: 39652540 PMC: 11627365. DOI: 10.1371/journal.pbio.3002437.


The role of polarization and early heterogeneities in the mammalian first cell fate decision.

Lamba A, Zernicka-Goetz M Curr Top Dev Biol. 2023; 154:169-196.

PMID: 37100517 PMC: 10291876. DOI: 10.1016/bs.ctdb.2023.02.006.


Aurora A and cortical flows promote polarization and cytokinesis by inducing asymmetric ECT-2 accumulation.

Longhini K, Glotzer M Elife. 2022; 11.

PMID: 36533896 PMC: 9799973. DOI: 10.7554/eLife.83992.


A combined and approach to the structure-function annotation of SPD-2 provides mechanistic insight into its functional diversity.

Murph M, Singh S, Schvarzstein M Cell Cycle. 2022; 21(18):1958-1979.

PMID: 35678569 PMC: 9415446. DOI: 10.1080/15384101.2022.2078458.


PLK-1 Regulation of Asymmetric Cell Division in the Early Embryo.

Kim A, Griffin E Front Cell Dev Biol. 2021; 8:632253.

PMID: 33553173 PMC: 7859328. DOI: 10.3389/fcell.2020.632253.


References
1.
Srayko M, Quintin S, Schwager A, Hyman A . Caenorhabditis elegans TAC-1 and ZYG-9 form a complex that is essential for long astral and spindle microtubules. Curr Biol. 2003; 13(17):1506-11. DOI: 10.1016/s0960-9822(03)00597-9. View

2.
Wallenfang M, Seydoux G . Polarization of the anterior-posterior axis of C. elegans is a microtubule-directed process. Nature. 2000; 408(6808):89-92. DOI: 10.1038/35040562. View

3.
Hao Y, Boyd L, Seydoux G . Stabilization of cell polarity by the C. elegans RING protein PAR-2. Dev Cell. 2006; 10(2):199-208. PMC: 1712613. DOI: 10.1016/j.devcel.2005.12.015. View

4.
Le Bot N, Tsai M, Andrews R, Ahringer J . TAC-1, a regulator of microtubule length in the C. elegans embryo. Curr Biol. 2003; 13(17):1499-505. DOI: 10.1016/s0960-9822(03)00577-3. View

5.
Brenner S . The genetics of Caenorhabditis elegans. Genetics. 1974; 77(1):71-94. PMC: 1213120. DOI: 10.1093/genetics/77.1.71. View