scholarly journals THE DEVELOPMENT OF BASAL BODIES AND FLAGELLA IN ALLOMYCES ARBUSCULUS

1964 ◽  
Vol 23 (2) ◽  
pp. 339-354 ◽  
Author(s):  
Fernando L. Renaud ◽  
Hewson Swift
Keyword(s):  
Electron Microscope ◽  
Basal Body ◽  
De Novo ◽  
The Other ◽  
Basal Bodies ◽  
Distilled Water ◽  
Vegetative Hypha ◽  
Original Length ◽  
Large Primary ◽  
Hyphal Tip

The development of basal bodies and flagella in the water mold Allomyces arbusculus has been studied with the electron microscope. A small pre-existing centriole, about 160 mµ in length, was found in an inpocketing of the nuclear membrane in the vegetative hypha. Thus, formation of a basal body does not occur de novo. When the hyphal tip started to differentiate into gametangia, the centrioles were found to exist in pairs. One of the members of the pair then grew distally to more than three times its original length, whereas the other remained the same size. The larger centriole would correspond to the basal body of a future gamete. Gametogenesis was usually induced by transferring a "ripe" culture to distilled water. Shortly after this was done, a few vesicles were pinched off from the cell membrane of the gametangium and came in contact with the basal body. Apparently, they fused and formed a large primary vesicle. The flagellum then started to grow by invaginating into it. Flagellar fibers were evident from the very beginning. As the flagellum grew so did the vesicle by fusion with secondary vesicles, thus coming to form the flagellar sheath. The different stages of flagellar morphogenesis are described and the possible interrelationships with other processes are discussed.

scholarly journals THE NUCLEIC ACIDS OF BASAL BODIES ISOLATED FROM TETRAHYMENA PYRIFORMIS

1965 ◽  
Vol 25 (2) ◽  
pp. 217-228 ◽  
Author(s):  
Eugene J. Hoffman
Keyword(s):  
Electron Microscope ◽  
Nucleic Acids ◽  
Basal Body ◽  
Tetrahymena Pyriformis ◽  
Isolation Procedure ◽  
Basal Bodies ◽  
Phenol Extraction ◽  
Body Self

Pellicular fragments were isolated from ethanol-fixed cells of the holotrichous ciliate Tetrahymena pyriformis by the action of digitonin. The isolated pellicles were further fragmented and the basal bodies of the cilia isolated from them by three methods. The preparations, examined in the electron microscope as embedded sections or negatively stained samples, consisted mainly of somewhat deformed pellicular material, the bulk of which was basal body. DNA was determined by the diphenylamine method and by reaction with DNase, and RNA, by the orcinol method. Nucleic acids were isolated by phenol extraction and analyzed spectrophotometrically and by reaction with RNase. The assays indicated 1.2 to 2.6 per cent RNA, similar to previously published work, but only 0.0 to 1.0 per cent DNA, near enough the sensitivity limits to render the presence of DNA in the preparations uncertain. Although the isolation procedure removed nuclear contents and ribosomes, the nucleic acids could still be a residual contaminant bound to the pellicle during the isolation. Hypotheses of basal body self-duplication, moreover, can be constructed both with and without nucleic acids.

Ultrastructure of the flagellar roots in Chlamydomonas gametes

1984 ◽  
Vol 67 (1) ◽  
pp. 133-143
Author(s):  
R.L. Weiss
Keyword(s):  
Basal Body ◽  
Direct Contact ◽  
The Other ◽  
Basal Bodies ◽  
Flagellar Roots ◽  
Mating Structure ◽  
Membrane Extension ◽  
Microtubular Root ◽  
Basal Apparatus ◽  
Microtubular System

The cytoskeleton of Chlamydomonas reinhardtii gametes has been studied by electron microscopy. The microtubular system, consisting of four flagellar roots inserted into the basal apparatus, is shown to include two daughter basal bodies and two striated fibres, newly described in this report. One new fibre associates with the 3-over-1 root and is similar to its counterpart, the striated fibre of the 2-member root. These similar root fibres connect each daughter basal body to the V-shaped microtubular root pair. The other new striated fibre joins the daughter basal body to both flagellar roots and is similar to the proximal striated fibre. In mt+ gametes, the conventional root microtubules make direct contact with the doublet zone of the non-activated mating structure. During activation, doublet zone microfilaments associate with the daughter basal body and the finely striated fibre of the 3-over-1 root. These observations suggest that the cytoskeleton acts as a scaffolding for membrane extension by the mt+ mating structure microfilaments.

scholarly journals De novo formation of basal bodies in Naegleria gruberi

2005 ◽  
Vol 169 (5) ◽  
pp. 719-724 ◽  
Author(s):  
Hong-Kyung Kim ◽  
Jeong-Gu Kang ◽  
Shigehiko Yumura ◽  
Charles J. Walsh ◽  
Jin Won Cho ◽  
...  
Keyword(s):  
Western Blotting ◽  
Basal Body ◽  
Gel Electrophoresis ◽  
De Novo ◽  
Myosin Ii ◽  
Basal Bodies ◽  
2D Gel Electrophoresis ◽  
2D Gel ◽  
Naegleria Gruberi

The de novo formation of basal bodies in Naegleria gruberi was preceded by the transient formation of a microtubule (MT)-nucleating complex containing γ-tubulin, pericentrin, and myosin II complex (GPM complex). The MT-nucleating activity of GPM complexes was maximal just before the formation of visible basal bodies and then rapidly decreased. The regulation of MT-nucleating activity of GPM complexes was accomplished by a transient phosphorylation of the complex. Inhibition of dephosphorylation after the formation of basal bodies resulted in the formation of multiple flagella. 2D-gel electrophoresis and Western blotting showed a parallel relationship between the MT-nucleating activity of GPM complexes and the presence of hyperphosphorylated γ-tubulin in the complexes. These data suggest that the nucleation of MTs by GPM complexes precedes the de novo formation of basal bodies and that the regulation of MT-nucleating activity of GPM complexes is essential to the regulation of basal body number.

Ultrastructure and development of the flagellar apparatus and flagellar motion in the colonial graeen alga Astrephomene gubernaculifera

1983 ◽  
Vol 63 (1) ◽  
pp. 21-41
Author(s):  
H.J. Hoops ◽  
G.L. Floyd
Keyword(s):  
Basal Body ◽  
Rotational Symmetry ◽  
Amorphous Material ◽  
Flagellar Apparatus ◽  
The Other ◽  
Basal Bodies ◽  
Mature Cell ◽  
Embryonic Cleavage ◽  
Development Proceeds ◽  
Concurrent Events

Immediately following embryonic cleavage, the cells of Astrephomene have four equal-sized basal bodies, two of which are connected by a striated distal fibre and two striated proximal fibres. The four microtubular rootlets, which alternate between having 3/1 and 2 members, are arranged cruciately. The two basal bodies that are connected by the striated fibres then extend into flagella, while the two accessory basal bodies are now markedly shorter. At this stage the flagellar apparatus has 180 degrees rotational symmetry and is very similar to the flagellar apparatus of the unicellular Chlamydomonas and related algae. Development proceeds with a number of concurrent events. The basal bodies begin to separate at their proximal ends and become nearly parallel. Each striated proximal fibre detaches at one end from one of the basal bodies. Each half of the flagellar apparatus, which consists of a flagellum and attached basal body, an accessory basal body, two rootlets and a striated fibre (formerly one of the proximal striated fibres), rotates about 90 degrees, the two halves rotating in opposite directions. An electron-dense strut forms near one two-membered rootlet and grows past both basal bodies. During this time a fine, fibrous component appears between newly developed spade-like structures and associated amorphous material connected to each basal body. The basal bodies continue to separate as the distal fibre stretches and finally detaches from one of them. These processes result in the loss of the 180 degree rotational symmetry present in previous stages. Although the flagella continue to separate, there is no further reorganization of the components of the flagellar apparatus. In the mature cell of Astrephomene, the two flagella are inserted separately and are parallel. The four microtubular rootlets are no longer arranged cruciately. Three of the rootlets are nearly parallel, while the fourth is approximately perpendicular to the other three. A straited fibre connects each basal body to the underside of the strut. These fibres run in the direction of the effective stroke of the flagella and might be important either in anchoring the basal bodies or in the initiation of flagellar motion. Unlike the case in the unicellular Chlamydomonas, the two flagella beat in the same direction and in parallel planes. The flagella of a given cell may or may not beat in synchrony. The combination of this type of flagellar motion and the parallel, separate flagella appears to be suited to the motion of this colonial organism.

scholarly journals Emerging Picture of Deuterosome-Dependent Centriole Amplification in MCCs

Cells ◽  
2018 ◽  
Vol 7 (10) ◽  
pp. 152 ◽  
Author(s):  
Umama Shahid ◽  
Priyanka Singh
Keyword(s):  
Basal Body ◽  
De Novo ◽  
Super Resolution ◽  
Basal Bodies ◽  
Parallel Pathways ◽  
Multiciliated Cells ◽  
Dependent Pathway ◽  
Microtubule Structure

Multiciliated cells (MCCs) have several hair-like structures called cilia, which are required to propel substances on their surface. A cilium is organized from a basal body which resembles a hollow microtubule structure called a centriole. In terminally differentiated MCCs, hundreds of new basal bodies/centrioles are formed via two parallel pathways: the centriole- and deuterosome-dependent pathways. The deuterosome-dependent pathway is also referred to as “de novo” because unlike the centriole-dependent pathway which requires pre-existing centrioles, in the de novo pathway multiple new centrioles are organized around non-microtubule structures called deuterosomes. In the last five years, some deuterosome-specific markers have been identified and concurrent advancements in the super-resolution techniques have significantly contributed to gaining insights about the major stages of centriole amplification during ciliogenesis. Altogether, a new picture is emerging which also challenges the previous notion that deuterosome pathway is de novo. This review is primarily focused on studies that have contributed towards the better understanding of deuterosome-dependent centriole amplification and presents a developing model about the major stages identified during this process.

scholarly journals Basal Body Duplication and Maintenance Require One Member of the Tetrahymena thermophila Centrin Gene Family

2005 ◽  
Vol 16 (8) ◽  
pp. 3606-3619 ◽  
Author(s):  
Alexander J. Stemm-Wolf ◽  
Garry Morgan ◽  
Thomas H. Giddings ◽  
Erin A. White ◽  
Robb Marchione ◽  
...  
Keyword(s):  
Basal Body ◽  
Calcium Binding ◽  
Tetrahymena Thermophila ◽  
Essential Gene ◽  
Expression Patterns ◽  
Spindle Pole ◽  
The Other ◽  
Basal Bodies ◽  
Spindle Pole Bodies ◽  
Ef Hand

Centrins, small calcium binding EF-hand proteins, function in the duplication of a variety of microtubule organizing centers. These include centrioles in humans, basal bodies in green algae, and spindle pole bodies in yeast. The ciliate Tetrahymena thermophila contains at least four centrin genes as determined by sequence homology, and these have distinct localization and expression patterns. CEN1's role at the basal body was examined more closely. The Cen1 protein localizes primarily to two locations: one is the site at the base of the basal body where duplication is initiated. The other is the transition zone between the basal body and axoneme. CEN1 is an essential gene, the deletion of which results in the loss of basal bodies, which is likely due to defects in both basal body duplication and basal body maintenance. Analysis of the three other centrins indicates that two of them function at microtubule-rich structures unique to ciliates, whereas the fourth is not expressed under conditions examined in this study, although when artificially expressed it localizes to basal bodies. This study provides evidence that in addition to its previously known function in the duplication of basal bodies, centrin is also important for the integrity of these organelles.

scholarly journals REGULATION OF MICROTUBULES IN TETRAHYMENA

1973 ◽  
Vol 56 (2) ◽  
pp. 458-465 ◽  
Author(s):  
Norman E. Williams ◽  
E. Marlo Nelsen
Keyword(s):  
Basal Body ◽  
De Novo ◽  
Basal Bodies ◽  
De Novo Synthesis

Experiments are reported which were designed to test for induced synthesis of microtubule proteins associated with the rapid proliferation of basal bodies and associated intracytoplasmic microtubules which occurs during oral replacement in Tetrahymena. None was found. Instead, it is shown that these structures can be formed with de novo synthesis of as little as 6% of their microtubule proteins. It is suggested that basal body proliferation may be controlled by synthesis of morphogenetic regulator proteins.

scholarly journals STUDIES OF SPERMATOGENESIS IN THE HEPATICAE

1968 ◽  
Vol 36 (3) ◽  
pp. 603-616 ◽  
Author(s):  
Zane B. Carothers ◽  
Gerald L. Kreitner
Keyword(s):  
Basal Body ◽  
Composite Structure ◽  
Narrow Band ◽  
Lateral Displacement ◽  
The Other ◽  
Marchantia Polymorpha ◽  
Basal Bodies ◽  
Stage Of Development ◽  
Uppermost Layer

The blepharoplast in a young, developing spermatid of Marchantia polymorpha, is a composite structure consisting of two basal bodies and a subjacent narrow band of axonemal-type tubules that we have termed the "spline." For most of its length, the spline consists of six long parallel tubules that nearly encircle the cell. The spline anterior is asymmetrically widened for about 2 µ by shorter tubules of the same kind. The lateral displacement of three long, adjacent marginal tubules by three short intervening tubules at the spline tip produces a long narrow aperture. Distally, the aperture is closed by the convergence of the displaced tubules with another trio of long tubules. Together, these form the six-membered cell-encircling portion. The expanded spline anterior has, at this stage of development, the four-layered (Vierergruppe) structure, of which the aforementioned tubules constitute the uppermost layer. The lower three strata consist of diagonal fins, elongated chambers, and fine tubules, respectively. The two flagellar bases lie close above the spline tip—one slightly anterior to the other—and diverge unequally from the spline axis. A few triplets extend proximally from the basal bodies, but do not connect with the spline. The anterior basal body is longer than the posterior one.

scholarly journals Naegleria gruberi De Novo Basal Body Assembly Occurs via Stepwise Incorporation of Conserved Proteins

2010 ◽  
Vol 9 (6) ◽  
pp. 860-865 ◽  
Author(s):  
Lillian K. Fritz-Laylin ◽  
Zoe June Assaf ◽  
Sean Chen ◽  
W. Zacheus Cande
Keyword(s):  
Basal Body ◽  
De Novo ◽  
Unicellular Eukaryote ◽  
Basal Bodies ◽  
Microtubule Cytoskeleton ◽  
Cytoplasmic Microtubule ◽  
Content Type ◽  
Genes Encoding ◽  
Associated Proteins ◽  
Naegleria Gruberi

ABSTRACT Centrioles and basal bodies are discrete structures composed of a cylinder of nine microtubule triplets and associated proteins. Metazoan centrioles can be found at mitotic spindle poles and are called basal bodies when used to organize microtubules to form the core structure of flagella. Naegleria gruberi, a unicellular eukaryote, grows as an amoeba that lacks a cytoplasmic microtubule cytoskeleton. When stressed, Naegleria rapidly (and synchronously) differentiates into a flagellate, forming a complete cytoplasmic cytoskeleton de novo, including two basal bodies and flagella. Here, we show that Naegleria has genes encoding conserved centriole proteins. Using novel antibodies, we describe the localization of three centrosomal protein homologs (SAS-6, γ-tubulin, and centrin-1) during the assembly of the flagellate microtubule cytoskeleton. We also used these antibodies to show that Naegleria expresses the proteins in the same order as their incorporation into basal bodies, with SAS-6 localizing first, followed by centrin and finally γ-tubulin. The similarities between basal body assembly in Naegleria and centriole assembly in animals indicate that mechanisms of assembly, as well as structure, have been conserved throughout eukaryotic evolution.

The Spindle as a Basal Body Distributor

1970 ◽  
Vol 7 (1) ◽  
pp. 65-89
Author(s):  
M. FRIEDLÄNDER ◽  
J. WAHRMAN
Keyword(s):  
Cell Cycle ◽  
Endoplasmic Reticulum ◽  
Basal Body ◽  
De Novo ◽  
The State ◽  
Basal Bodies ◽  
Metaphase Chromosomes ◽  
Silk Moth ◽  
Combined Mechanism

The spindle of metazoan cells functions as a dual distributor that guarantees the accurate segregation of both chromosomes and centrioles (basal bodies). This combined mechanism may have evolved from the separate distribution devices for chromosomes and basal bodies found in Protozoa. Typical eupyrene spermatocytes of the silk moth were compared with atypical apyrene spermatocytes. (a) Long microtubules, persisting during centriolar movements, develop in the meiotic prophases in continuity with the centrioles (b) There is no longer a centriole-microtubule continuity at metaphase-anaphase (c) Spindles comprise microtubules and endoplasmic reticulum (ER). The microtubules form a barrel-shaped structure terminating far in front of the centrioles. The two types of spermatocytes differ in the structure of the ER, which is vesicular in the eupyrene and lamellar in the apyrene line. It is suggested that the ER influences the anaphase movement of chromosomes, (d) The chromosomes lack localized centromeres. Microtubules penetrate all along the polar faces of the eupyrene metaphase chromosomes. The apyrene chromosomes form irregular blocks that are penetrated by microtubules all around their periphery, (e) The centriole comprises 3 concentric zones. Typical changes in the centriole are correlated with changes in the cell cycle. Replication, de novo formation and disappearance of centrioles are manifestations of the state of flux of the microtubules.

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