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 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 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 HEATH, I. B.
Right arrow Articles by KAMINSKYJ, S. G.W.
Right arrow Search for Related Content
PubMed
Right arrow Articles by HEATH, I. B.
Right arrow Articles by KAMINSKYJ, S. G.W.
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 93, 41-52, Copyright © 1989 by Company of Biologists

Submitted on January 9, 1989
Accepted on February 15, 1989

The organization of tip-growth-related organelles and microtubules revealed by quantitative analysis of freeze-substituted oomycete hyphae

I. BRENT HEATH 1 and SUSAN G.W. KAMINSKYJ 1

1 Biology Department, York University 4700 Keele Street, North York, Ontario, Canada M3J 1P3

The distribution of organelles and microtubules in hyphal tips of the oomycete, Saprolegnia ferax, were quantitatively determined at high resolution from serial-section electron microscopy of freeze-substituted cells. All the organelles and the microtubules were non-uniformly distributed, each showing a characteristic longitudinal gradient starting at a different point behind the tip. In addition, when the cytoplasmic cross-sectional area was divided into radial regions, all organelles occurred preferentially in either the central (mitochondria and Golgi bodies) or the peripheral (microtubules, wall vesicles and spherical vesicles) region. The nuclei were so large as to span both regions but were always oriented with their centrioles facing the plasmalemma. Microtubules occurred in the extreme tips, became more abundant sub-apically, were predominantly short but increased in mean length with distance from the tip. The correlated patterns of organelle and cytoskeleton organization from this and previous work show that neither the microtubules nor the detected arrays of actin are sufficient to account for most organelle arrangements. However, on the basis of the distribution and orientation of the predominantly elongated wall vesicles, we suggest that the wall vesicles travel radially from their origin at the centrally located Golgi bodies to the cell periphery where they are transported longitudinally to the hyphal tip in conjunction with the plasmalemma-associated actin cables. Our data also suggest that the hyphae contain a cortical ectoplasm with which the nuclei interact, at least in part, via their centrioles and centriole-associated microtubules, and whose mechanical integrity is increased by both the peripheral actin cables and a high density of microtubules. We suggest that the endoplasm is less strong and has physiological properties that enhance the differentiation of endoplasmic reticulum and nuclear envelope into Golgi body production.

Key words: tip growth, microtubules, actin, organelles, organelle motility

Submitted on January 9, 1989
Accepted on February 15, 1989


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
MicrobiologyHome page
M. A. Hubbard and S. G. W. Kaminskyj
Rapid tip-directed movement of Golgi equivalents in growing Aspergillus nidulans hyphae suggests a mechanism for delivery of growth-related materials
Microbiology, May 1, 2008; 154(5): 1544 - 1553.
[Abstract] [Full Text] [PDF]


Home page
MicrobiologyHome page
K. Sampson and I. B. Heath
The dynamic behaviour of microtubules and their contributions to hyphal tip growth in Aspergillus nidulans
Microbiology, May 1, 2005; 151(5): 1543 - 1555.
[Abstract] [Full Text] [PDF]


Home page
Plant Cell PhysiolHome page
Y. P. Yu, S. L. Jackson, and A. Garrill
Two Distinct Distributions of F-actin are Present in the Hyphal Apex of the Oomycete Achlya bisexualis
Plant Cell Physiol., March 15, 2004; 45(3): 275 - 280.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
C Bachewich and I. Heath
Radial F-actin arrays precede new hypha formation in Saprolegnia: implications for establishing polar growth and regulating tip morphogenesis
J. Cell Sci., June 8, 2000; 111(14): 2005 - 2016.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
S. Kaminskyj and I. Heath
Integrin and spectrin homologues, and cytoplasm-wall adhesion in tip growth
J. Cell Sci., January 2, 1995; 108(2): 849 - 856.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
N. Levina, R. Lew, and I. Heath
Cytoskeletal regulation of ion channel distribution in the tip-growing organism Saprolegnia ferax
J. Cell Sci., January 1, 1994; 107(1): 127 - 134.
[Abstract] [PDF]


Home page
J. Cell Sci.Home page
G Steinberg and M Schliwa
Organelle movements in the wild type and wall-less fz;sg;os-1 mutants of Neurospora crassa are mediated by cytoplasmic microtubules
J. Cell Sci., January 10, 1993; 106(2): 555 - 564.
[Abstract] [PDF]




© The Company of Biologists Ltd 1989