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

1989 ◽  
Vol 93 (1) ◽  
pp. 41-52
Author(s):  
I. BRENT HEATH ◽  
SUSAN G.W. KAMINSKYJ
Keyword(s):  
Golgi Body ◽  
Cell Periphery ◽  
Cross Sectional ◽  
Saprolegnia Ferax ◽  
Cytoskeleton Organization ◽  
Golgi Bodies ◽  
Section Electron ◽  
Serial Section Electron Microscopy ◽  
Body Production ◽  
Actin Cables

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.

Nuclear cycle of Saprolegnia ferax

1981 ◽  
Vol 49 (1) ◽  
pp. 353-367
Author(s):  
I.B. Heath ◽  
K. Rethoret
Keyword(s):  
Electron Microscopy ◽  
Dna Synthesis ◽  
Single Group ◽  
Saprolegnia Ferax ◽  
Opposite Pole ◽  
Nuclear Cycle ◽  
Section Electron ◽  
Serial Section Electron Microscopy ◽  
Inhibition Of Dna Synthesis ◽  
Section Electron Microscopy

The mitotic nuclear (equivalent to cell) cycle of the oomycete fungus, Saprolegnia ferax, was analysed by quantitative serial-section electron microscopy of hyphal nuclear populations synchronized by inhibition of DNA synthesis by fluorodeoxyuridine (FdUrd). Following telophase and karyokinesis, kinetochore mitrotubules persist into G1 stage as a single group of approximately 42 per nucleus (2n = 42 for this species). During G1 the centrioles replicate and kinetochore microtubules separate into 2 groups of approximately 21, a configuration they retain through S and G2. During metaphase a new population of kinetochore microtubules are formed, each one of an amphitelic pair connecting to the opposite pole to that associated with the persistent microtubule from the previous division. Thus, by the end of metaphase, there are approximately 42 kinetochore microtubules per half spindle. FdUrd, applied for 2 h with uracil, completely blocks DNA synthesis yet permits centriole replication and causes nuclei to accumulate with 2 pairs of centrioles, 2 arrays (each of 21) of kinetochore microtubules, and apparently enlarged nucleoli. Removal of FdUrd permits rapid (within 30 min) DNA synthesis followed by successive rounds of decreasingly synchronous nuclear cycles. These post-FdUrd cycles are 2.5 times longer than normal at 2.5 h, with S plus G2 being more extended than other phases. Calculated durations of a normal nuclear cycle are: G1, 33 min; S, 7 min; G2, 10 min; metaphase, 8 min; anaphase, 0.5 min; and telophase, 4 min.

Normal Synaptonemal Complex and Abnormal Recombination Nodules in Two Alleles of the Drosophila Meiotic Mutant mei-W68

Genetics ◽  
2003 ◽  
Vol 163 (4) ◽  
pp. 1337-1356 ◽  
Author(s):  
Adelaide T C Carpenter
Keyword(s):  
Electron Microscopy ◽  
Synaptonemal Complex ◽  
High Frequency ◽  
Serial Section ◽  
The Other ◽  
Wild Type ◽  
Recombination Nodules ◽  
Section Electron ◽  
Serial Section Electron Microscopy ◽  
Section Electron Microscopy

Abstract The meiotic phenotypes of two mutant alleles of the mei-W68 gene, 1 and L1, were studied by genetics and by serial-section electron microscopy. Despite no or reduced exchange, both mutant alleles have normal synaptonemal complex. However, neither has any early recombination nodules; instead, both exhibit high numbers of very long (up to 2 μm) structures here named “noodles.” These are hypothesized to be formed by the unchecked extension of identical but much shorter structures ephemerally seen in wild type, which may be precursors of early recombination nodules. Although the mei-W68L1 allele is identical to the mei-W681 allele in both the absence of early recombination nodules and a high frequency of noodles (i.e., it is amorphic for the noodle phene), it is hypomorphic in its effects on exchange and late recombination nodules. The differential effects of this allele on early and late recombination nodules are consistent with the hypothesis that Drosophila females have two separate recombination pathways—one for simple gene conversion, the other for exchange.

Ultrastructure of the female reproductive organs (ovary, vitellaria, and Mehlis' gland) of Halipegus eccentricus (Trematoda: Derogenidae)

1986 ◽  
Vol 64 (10) ◽  
pp. 2203-2212 ◽  
Author(s):  
Jon M. Holy ◽  
Darwin D. Wittrock
Keyword(s):  
Cell Types ◽  
Reproductive Organs ◽  
Golgi Body ◽  
Digenetic Trematode ◽  
Secretory Cells ◽  
Cortical Granules ◽  
Golgi Bodies ◽  
Transmission Electron ◽  
Vitelline Cells ◽  
Female Reproductive Organs

The female reproductive organs (ovary, vitellaria, and Mehlis' gland) of the digenetic trematode Halipegus eccentricus were studied by transmission electron microscopy. Oocytes entered diplotene while in the ovary and produced cortical granules and lipid bodies. Vitelline cells produced large amounts of eggshell protein but no yolk bodies. Two types of Mehlis' gland secretory cells were present, distinguishable by the morphology of their rough endoplasmic reticulum, Golgi bodies, and secretory bodies, and by the persistence of recognizable secretory material within the ootype lumen after exocytosis. In an attempt to standardize the nomenclature regarding the cell types of the Mehlis' gland, a classification that takes into account these four criteria is proposed. Two basic types of Golgi body organization were noted for the cells of the female reproductive system: a stack of flattened cisternae (Mehlis' gland alpha cells) and spherical Golgi bodies with vesicular cisternae (oocytes, vitelline cells, and Mehlis' gland beta cells).

scholarly journals Golgi Body Motility in the Plant Cell Cortex Correlates with Actin Cytoskeleton Organization

2011 ◽  
Vol 52 (10) ◽  
pp. 1844-1855 ◽  
Author(s):  
Miriam Akkerman ◽  
Elysa J. R. Overdijk ◽  
Jan H. N. Schel ◽  
Anne Mie C. Emons ◽  
Tijs Ketelaar
Keyword(s):  
Actin Cytoskeleton ◽  
Plant Cell ◽  
Golgi Body ◽  
Cell Cortex ◽  
Cytoskeleton Organization ◽  
Actin Cytoskeleton Organization ◽  
Body Motility

Polyneuronal innervation of an adult and embryonic lobster muscle

Development ◽  
1985 ◽  
Vol 87 (1) ◽  
pp. 13-26
Author(s):  
c. K. Govind ◽  
Philip J. Stephens ◽  
Judith S. Eisen
Keyword(s):  
Homarus Americanus ◽  
Inhibitory Synapses ◽  
Neuromuscular Synapses ◽  
Extensor Muscles ◽  
Full Complement ◽  
Section Electron ◽  
Innervation Patterns ◽  
The Common ◽  
Serial Section Electron Microscopy ◽  
Polyneuronal Innervation

Motor innervation of the deep extensor muscle in the abdomen of lobsters (Homarus americanus) was compared in adults and embryos using electrophysiological techniques. There is widespread innervation of the adult muscle by the common excitor and inhibitor axons and regionally restricted or private innervation by three more excitor axons. In the embryo the earliest sign of functional innervation revealed a single inhibitory and two to three excitatory axons thus denoting simultaneous innervation by the full complement of axons. In corroboration, serial-section electron microscopy revealed several axon profiles invading the embryonic deep extensor muscles and giving rise to well-defined neuromuscular synapses with presynaptic dense bars. Innervation patterns to homologous regions of the embryonic and adult muscles were similar, consisting of a few large inhibitory synapses and many small excitatory ones. Consequently the adult pattern of polyneuronal innervation occurs simultaneously and in toto during embryonic development.

The Golgi Material and Mitochondria in the Salivary Glands of the Larva of Drosophila Melanogaster

1948 ◽  
Vol s3-89 (8) ◽  
pp. 401-414
Author(s):  
W. SIANG HSU
Keyword(s):  
Salivary Glands ◽  
Golgi Body ◽  
Anterior Portion ◽  
Golgi Bodies ◽  
Gland Cells ◽  
Salivary Gland Cells ◽  
Visible Part ◽  
Show Evidence ◽  
Storage Granules ◽  
Reserve Food

1. The salivary glands in the larvae of Drosophila show evidence of serving two functions: (1) production of digestive secretion, (2) accumulation of reserve food for the period of pupation. The two functions proceed simultaneously within the same cell during certain stages of its development. 2. A single droplet of digestive material has been seen to originate and grow within each Golgi body in the gland-cells. When a certain size is reached the droplet is released into the cytoplasm and by the fusion of two or more of them bigger vacuoles are formed. The secretory material is discharged into the lumen by means of a merocrine mechanism. Neither mitochondria nor nucleus has been observed to take any visible part in the elaboration of secretion droplets. 3. The storage granules found in older and larger cells have been observed to be direct transformations of chondriomites, and neither the Golgi material nor the nucleus shows any sign of participation in the formation of these granules. 4. From the standpoint of morphology and behaviour, the Golgi bodies found in the salivary gland cells are the same as found in the cells of the glandular portion of the proventriculus and the epithelium of the anterior portion of the midgut of the larva. 5. My observations do not lend themselves convincingly to a two-component conception of the structure of Golgi bodies.

scholarly journals Endomembrane architecture and dynamics during secretion of the extracellular matrix of the unicellular charophyte, Penium margaritaceum

2020 ◽  
Vol 71 (11) ◽  
pp. 3323-3339 ◽  
Author(s):  
David S Domozych ◽  
Li Sun ◽  
Kattia Palacio-Lopez ◽  
Reagan Reed ◽  
Susan Jeon ◽  
...  
Keyword(s):  
Extracellular Matrix ◽  
Brefeldin A ◽  
Extracellular Polysaccharide ◽  
Sister Group ◽  
Golgi Body ◽  
Endomembrane System ◽  
Golgi Bodies ◽  
Cytoplasmic Vesicles ◽  
Structural Details ◽  
Colonization Of Land

Abstract The extracellular matrix (ECM) of many charophytes, the assemblage of green algae that are the sister group to land plants, is complex, produced in large amounts, and has multiple essential functions. An extensive secretory apparatus and endomembrane system are presumably needed to synthesize and secrete the ECM, but structural details of such a system have not been fully characterized. Penium margaritaceum is a valuable unicellular model charophyte for studying secretion dynamics. We report that Penium has a highly organized endomembrane system, consisting of 150–200 non-mobile Golgi bodies that process and package ECM components into different sets of vesicles that traffic to the cortical cytoplasm, where they are transported around the cell by cytoplasmic streaming. At either fixed or transient areas, specific cytoplasmic vesicles fuse with the plasma membrane and secrete their constituents. Extracellular polysaccharide (EPS) production was observed to occur in one location of the Golgi body and sometimes in unique Golgi hybrids. Treatment of cells with brefeldin A caused disruption of the Golgi body, and inhibition of EPS secretion and cell wall expansion. The structure of the endomembrane system in Penium provides mechanistic insights into how extant charophytes generate large quantities of ECM, which in their ancestors facilitated the colonization of land.

scholarly journals Centriolar remodeling underlies basal body maturation during ciliogenesis in Caenorhabditis elegans

eLife ◽  
2017 ◽  
Vol 6 ◽  
Author(s):  
Inna V Nechipurenko ◽  
Cristina Berciu ◽  
Piali Sengupta ◽  
Daniela Nicastro
Keyword(s):  
Electron Microscopy ◽  
High Resolution ◽  
Sensory Neurons ◽  
Basal Body ◽  
Three Dimensional ◽  
C Elegans ◽  
Mother Centriole ◽  
Section Electron ◽  
Serial Section Electron Microscopy ◽  
Section Electron Microscopy

The primary cilium is nucleated by the mother centriole-derived basal body (BB) via as yet poorly characterized mechanisms. BBs have been reported to degenerate following ciliogenesis in the C. elegans embryo, although neither BB architecture nor early ciliogenesis steps have been described in this organism. In a previous study (Doroquez et al., 2014), we described the three-dimensional morphologies of sensory neuron cilia in adult C. elegans hermaphrodites at high resolution. Here, we use serial section electron microscopy and tomography of staged C. elegans embryos to demonstrate that BBs remodel to support ciliogenesis in a subset of sensory neurons. We show that centriolar singlet microtubules are converted into BB doublets which subsequently grow asynchronously to template the ciliary axoneme, visualize degeneration of the centriole core, and define the developmental stage at which the transition zone is established. Our work provides a framework for future investigations into the mechanisms underlying BB remodeling.

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