The Positioning of Ciliary Organelles in Hypotrich Ciliates*†

It is commonly observed in hypotrichs that new ciliary rudiments arise directly from or in close juxtaposition to certain pre-existing ciliary elements. Oral primordia often are initiated near specific cirri, cirral rudiments frequently arise as a result of the disaggregation of certain old cirri, and new dorsal ciliature is formed within pre-existing ciliary rows. In the first 2 situations it has been demonstrated experimentally that neither the old ciliature in question nor the specific cortical site marked by that ciliature is essential for the appearance of the new cirral rudiment. The experimental analysis done thus far suggests that the positions of oral and cirral primordia are determined by interacting gradients established in relation to certain reference points. The nature of the reference points is not fully elucidated; in some cases at least these points appear to be more closely related to topographic features of the cell than to specific pre-existing cortical structures. In the dorsal ciliary rows of Euplotes new ciliary units are formed usually and perhaps invariably in close proximity to old ones, and are generally oriented along the axis of the pre-existing row. The result is a tendency to perpetuate the preexisting row number across cell generations. Changes in row number, however, can occur as a result of occasional formation of new units at right angles to the row, a process that is much enhanced in certain homozygous segregants (basal body deficient). The optimal row number (stability range) as well as the number of ciliary units are under genic control. In addition, the spatial pattern of distribution of ciliary units among rows is invariant in all of the material examined. This pattern is presumed to result from an underlying field whose geometry is independent of both the number of units and the number of rows.     

Development of the Ciliary Pattern of the Oral Apparatus of Tetrahymena thermophila1

ABSTRACT. The sequence of formation and ciliation of basal bodies and the subsequent organization of compound ciliary structures of the oral apparatus of Tetrahymena thermophila was reanalyzed with the aid of scanning electron microscopy of cells in which the epiplasmic layer was exposed, as well as by light microscopy of protargol-impregnated specimens. This combination of methods allowed the delineation of numerous steps in the patterning of the oral ciliature, some of which have received little or no previous attention. Highlights include: the initial formation of “strings” of nonciliated new basal bodies in juxtaposition to relatively few basal bodies of the stomatogenic kinety; generation of basal body pairs, roughly oriented along the anteroposterior axis of the cell, that later align side-by-side to assemble promembranelles; condensation and reorientation of promembranelles simultaneous with addition of a third row of basal bodies anterior to the original two rows; production of a very short fourth row of basal bodies at the anterior right end of each developing membranelle; generation of the outer basal body row of the undulating membrane (UM) after alignment of the inner row, with transient ciliation of the inner row preceding permanent ciliation of the outer row; limited basal body resorption at the ends of membranelles; and sculpturing of the right ends of membranelles by a movement of basal bodies associated with formation of the ribbed wall adjacent to the UM. In the old anterior oral apparatus a repetition of the processes of generation of a new outer UM row and sculpturing of right ends of membranelles takes place in synchrony with the corresponding events in the oral primordium, following prior shedding of the old outer UM row and loss of the sculptured pattern in association with temporary regression of the ribbed wall micro-tubules. Oral development is complex, with different processes involved in the assembly of the membranelles and the UM, and with a sequence of distinct events involved in the generation of each of these structures. Speaking comparatively, membranelle development follows the same pathway in many, perhaps all, ciliates in which these structures or their homologues develop from a common stomatogenic field.     

Structural deficiency of 180°-rotated ciliary rows in Tetrahymena: Implications on the inheritance and development of a non-genically acquired cortical trait during vegetative propagation

The present study reveals a deficiency in the number of ciliated basal bodies along 180° rotated ciliary rows (IRs) in Tetrahymena. This feature is common to IRs recently generated in young clones with stable corticotypes (total number of ciliary rows per cell), irrespective of the number of IRs present per cell or their cellular location, and is found before the cell loses any of the IRs. In cells bearing three IRs, the IRs on the two sides of the inversion immediately next to normal ciliary rows (junctures) exhibit an even greater deficiency in ciliated basal bodies, compared to the IR located internally between two other IRs; the normal ciliary rows flanking the inversion are also somewhat deficient. These observations show that the IRs of Tetrahymena are structurally deficient, hence developmentally defective, and suggest that they are intrinsically unstable. We propose that basal body development along IRs tends to be truncated before the stage of ciliation; such basal bodies would fail to acquire the potential to serve as nucleating centers for new basal body development in the next round of basal body proliferation, leading to the eventual loss of the IRs. © 1992 Wiley-Liss, Inc.     

The pattern of replication of cortical units in Tetrahymena

The patterns of increase in numbers of argentophilic elements (kinetosomes) are studied during the cell cycle of Tetrahymena pyriformis, syngen 1. The patterns suggest that new ciliary units are added uniformly to all ciliary rows during the early part of the cell cycle. After the start of the formation of the new oral apparatus, the rate of increase of the row to the right of the oral apparatus is increased and the rate of growth of the row to the left is decreased. The increase in total ciliary units, both somatic and oral, may well be constant for the entire cell cycle.     

The filaments supporting ciliary primordia and fission furrow in the hypotrich ciliateParaurostyla weissei, revealed by the monoclonal antibody 12G9: Studies on wild-type and ciliary hypertrophy mutant

Summary The unique monoclonal antibody FXXXIX 12G9 obtained againstTetrahymena cortices was used to label cytoskeletal structures related to basal body proliferation inParaurostyla weissei. The antibody binds to an amorphous material interconnecting basal bodies in compound ciliary structures: dorsal units, cirri and membranelles in interfission cells, and filamentous structures supporting the primordia of ciliary structures and fission line in dividing cells. The antibody visualized meridional filaments preceding proliferation of new basal bodies in the oral primordium and structures accompanying all developing ciliary primordia. It congregated in differentiating new procirri and membranelles, whereas another population of transient meridional structures accompanied the final distribution of new structures. A meridional filament connecting transverse cirri with the oral apparatus, marking the future stomatogenic meridian, persisted in both division products until completion of cell elongation. The fission line was found to originate from an anterior extension of the pre-oral filament toward the parental oral structures. It then encircled the cell's midbody demarcating the boundary between daughter cells; two additional circumferential structures bordering the anterior and posterior ends of differentiating division products participate in formation of the new poles. They disappear after separation of daughter cells and completion of resorption of parental ciliature. In the enhanced multi-left-marginal mutant expressing gross hyperduplication of basal bodies, the location of the 12G9 antigen corresponded to that in wild-type cells. The sequence of formation of meridional filaments in the mutant was found to be altered. The filaments in the left lateral domain preceded the formation of the preoral filament, yet the temporal pattern of basal body assembly was not modified. The fission line, as in wild-type cells, originated in connection with the oral primordium. We conclude that the nucleation of the filamentous structures bearing the 12G9 antigen and the basal body assembly occur by independent mechanisms reading the same cell cycle signals. We suggest that the 12G9-antigen-bearing protein might be similar to septins: involved in signaling the position of the oral primordium and the fission line and functioning in establishing and maintaining the asymmetric cortical domain characteristics.Abbrevations AZM zone of adorai membranelles - bb basal bodies - CC caudal cirri - FC frontal cirri - Fmf frontal meridional filament - FTV the primordia of fronto-ventro-transverse cirri - LD, RD dorsal rows of bristle units - LM, RM left or right marginal cirral row - OA oral apparatus - OP primordium of the adoral membranelles - pLM, pRM primordium of the left or right marginal cirri - pLD, pRD primordia of the left or right dorsal bristle rows - pUM primordium of the undulating membranes - TC transverse cirri - UM undulating membranes - VC ventral cirral rows     

Development of the ciliature of Tetrahymena thermophila: I. Temporal coordination with oral development

The number of basal bodies and cilia along pole-to-pole ciliary rows was enumerated in Tetrahymena thermophila cells sampled during the rapid-exponential phase of culture growth in three different media that supported generation times ranging from 2 to 4 hr. The time required for oral development was nearly constant in the three media, and thus most of the differences in generation time were accounted for by differences in the interval prior to the onset of oral development (stage 0), which ranged from 50% of the generation time in the “poorest” medium to 20% in the “richest.” There was very little increase in number of basal bodies and of cilia along ciliary rows during stage 0, irrespective of the duration of this stage. The bulk of the increase took place during oral development, following a time course suggestive of coordination wth oral development. The same temporal pattern of increase was found in several ciliary rows, although the proportion of basal bodies that were ciliated differed among rows. There is no simple relationship between the number of basal bodies along ciliary rows and cell length, surface area, or volume. However, a large and constant proportion of the total division-to-division cell growth took place during the interval prior to the onset of oral development, suggesting that an ensemble of developmental events, including oral development and an associated activation of the remainder of the cell surface, may be triggered by attainment of a threshold cell size.     

Hereditary variation of ciliary patterns in ciliated protozoa

Summary— In ciliates, the basic pattern of ciliature consists of longitudinal polarized ciliary rows. This basic pattern is expected to be retained through successive binary fissions by means of the so-called cytotactic mechanisms, as a consequence of autogenetic proliferation of basal bodies within each row. This idea is supported by the hereditary transmission of 180° rotated rows in Tetrahymena and Paramecium. These mechanisms should theoretically ensure intraclonal homogeneity for ciliary row number. In fact, some alterations are responsible for either loss or addition of rows. Such alterations are not strictly random processes, since they have been shown to be controlled by nuclear genes. Cytotaxis does not account for exact positioning of primordia for complex structures (buccal ciliature, for instance): the sites of basal body proliferation are determined by certain “positional information” which, in turn, is controlled by chromosomal genetic material more or less independently of pre-existing structures, as illustrated by many spontaneous or induced mutations. All deviations from the wild-type phenotype seem to be associated with very reduced fitness, at least in laboratory conditions. On the other hand, the currently known variants cannot account for intraspecific diversity. Thus, the evolutionary significance of these phenomena remains somewhat obscure.     

The formation of basal body domains in the membrane skeleton of Tetrahymena

Differentiated regions within the membrane skeleton are described around basal bodies in the ciliary rows of Tetrahymena. These domains, approximately 1 micron in diameter, are characterized by a relatively dense ultrastructure, the presence of a family of proteins called K antigens (Mr 39-44 x 10(3)) that are recognized by mAb 424A8, and the apparent exclusion of major membrane skeleton proteins that are present in most other regions of the cell (Mr 135, 125 x 10(3]. Mature basal body domains are asymmetric, reflecting the polarity of the cell as a whole. A similar differentiation of the membrane skeleton occurs in the oral apparatus, except here the K antigens surround four clusters of basal bodies (from which this cell takes its name) rather than the individual basal bodies. The development of new basal body domains in the cell cycle is described, with similarities and differences noted between somatic and oral regions of the cell. It is concluded that the capacity of this cell for precise topographic regulation of molecular events in the membrane skeleton makes it a useful model for the study of cortical differentiation in cells generally.     

Ultrastructure and cell size-dependent regulation of the adoral zone of membranelles in the heterotrich ciliate Stentor coeruleus

The number and length of oral membranelles were determined for both large and small Stentor from well-fed, growing cultures and nutrient-deprived cultures, respectively. Small cells possess both significantly fewer and shorter membranelles than do large cells. For both large and small cells, each membranelle is composed of three rows of basal bodies. The membranelles closest to the gullet have a third row that is only slightly shorter than the other two. The third row becomes rapidly shorter as membranelles become increasingly distant from the gullet. A short distance from the gullet, and for the remainder of the band, the third row is composed ofonly one to four basal bodies. The first two rows consist of approximately 35 basal bodies each in large cells and approximately 26 basal bodies each in small cells. This indicates that Stentor regulates the number of basal bodies per row, but not the number of rows, in response to changes in cell size. © 1992 Wiley-Liss, Inc.     

The Permanence of the Infraciliature in Suctoria: An Electronmicroscopic Study of Pattern Formation in Tokophrya infusionum*

SYNOPSIS. The adult Tokophrya infusionum does not possess cilia, but has 20–30 barren basal bodies arranged in 6 short rows adjacent to the contractile vacuole pore. During reproduction, which is by internal budding, the contractile vacuole sinks into the parent along with the invaginating membranes that form the embryo and the wall of the brood pouch. The 6 rows of basal bodies radiate away from the pore and elongate to form 5 long ciliary rows, that encircle the anterior half of the embryo, and 1 short row at the posterior end. The contractile vacuole pore, along with several barren basal bodies, remains in the parent when the embryo is completed. The pore rises to the surface when the embryo is born. New basal bodies are then formed in the parent to replace those which were incorporated into the embryo, and formation of another embryo may begin. The cilia of the embryo are partially resorbed 10 min after the start of metamorphosis, with depolymerization of the ciliary microtubules. Later, the cilia and most of the basal bodies disappear completely, except for a group of barren basal bodies near the embryo's contractile vacuole pore, which form 6 rows and serve as an anlage for the basal bodies and cilia that arise during embryogenesis. There is, therefore, an organized infraciliature in Suctoria throughout their life cycle, and a distinct continuity of basal bodies across the generations.     

Development of the ciliature of Tetrahymena thermophila: II. Spatial subdivision prior to cytokinesis

The cell surface of Tetrahymena thermophila is made up of an anterior region in which virtually all basal bodies of ciliary rows are ciliated, and the remainder in which ciliated and unciliated basal bodies are fairly irregularly interspersed. This pattern persists through interfission development until the stage of appearance of the equatorial ring of gaps in the ciliary rows that marks the fission zone. The ciliation pattern then becomes subdivided, in large part through the rapid ciliation of contiguous basal bodies located posterior to the fission zone. We interpret this process as a wave of ciliation of preexisting basal bodies that propagates posteriorly from the site of the fission zone. The location, extent, and timing of the ciliation process are the same in inverted as in normally oriented ciliary rows, in spite of the fact that in inverted rows the visible fission zone gap is tardily formed and the local configuration of ciliature around this gap is abnormal. The putative ciliation wave thus does not depend directly upon the local manifestations of the fission zone. However, in a cell-division-arrest mutant, cdaA1, analyzed under conditions in which formation of fission-zone gaps is permanently prevented in some ciliary rows but not in all, it is found that the ciliation pattern becomes subdivided in those ciliary rows that express fission-zone gaps and fails to become subdivided in neighboring rows that fail to manifest gaps. We interpret this combination of findings to indicate that a signal localized at the cell equator initiates a set of polarized developmental events that simultaneously create and demarcate two cellular fields within what was previously one. We further suggest that the characteristic tandem cell division pattern of ciliates is fundamentally a process of segmentation, which might involve mechanisms of gradient subdivision analogous to those taking place during segmentation of insects and other multicellular organisms.     

How the mirror-image pattern specified by a janus mutation of Tetrahymena thermophila comes to expression

The initial changes of cell-surface organization that occurred as the recessive janA1 (janus) mutation of Tetrahymena thermophila first became expressed were elucidated in a special mating scheme in which old macronuclei homozygous for janA+ were synchronously replaced by new macronuclei homozygous for janA1. During this period of onset of expression, the number, regularity, and asymmetry of the ciliary rows remained unchanged. New normal (primary) oral apparatuses (OAs) continued to be formed posterior to old OAs, as in normal cells. At about four fissions after conjugation, abnormal (secondary) OAs with a partial reversal of asymmetry began to appear nearly opposite to the primary OAs, close to but not at the eventual circumferential position of janA1 secondary OAs. The array of contractile vacuole pores (CVPs), normally located adjacent to two ciliary rows centered near 22% of the cell circumference to the right of the primary oral meridian, underwent a two-step transformation: first, the number of adjacent ciliary rows bearing CVPs increased to 3, 4, and sometimes 5, then "skipped" rows appeared within this broadened CVP-arc to split the single set of CVPs into two separated subsets. The CVP transformations occurred gradually and progressively. They began prior to the expression of secondary OAs but accelerated as secondary OAs appeared. As the CVP arc became broader, its midpoint shifted somewhat to the right, away from the primary oral meridian, but ended up close to halfway between the primary and secondary oral meridians. The data provide a better fit to an intercalation model than to an alternative double-gradient model, suggesting that the janA1 mutation alters the large-scale organization of positional values by preventing the expression of a subset of these values and thus provoking reverse-intercalation of the remainder.     

A genically determined abnormality in the number and arrangement of basal bodies in a ciliate

When an F₁ of a cross between clones K₇ and VF₁₇ of Euplotes minuta was backcrossed to the K₇ parent, 6 of the 30 progeny clones displayed a syndrome of abnormalities in cortical pattern, which included (1) substantial reduction in number of dorsal cilia, (2) a lesser reduction in number of ciliary rows, (3) absence of one or both right caudal cirri, (4) appearance of incomplete and abnormally oriented membranelle bases, (5) irregularities in form of ventral cirri. The length of cilia and arrangement of subpellicular fiber bundles were fully normal in these 6 clones, as were cell size and division rate. A test cross of one of these abnormal clones with the F₁ parent yielded a 1:1 segregation of normal and abnormal progeny clones, with no intermediate clones, suggesting a single-gene basis for the abnormal condition. Comparison of development in normal and abnormal clones suggested that the abnormal clones were defective in the formation of basal bodies; new basal bodies often failed to form at the expected sites, and occasionally appeared in atypical spatial relations to old basal bodies. As a probable consequence of this defect, the fidelity of cytoplasmic inheritance of preexisting ciliary row number, which was demonstrated to be considerable in normal clones, was reduced in the abnormal clones.     

Effect of alteration in the global body plan on the deployment of morphogenesis-related protein epitopes labeled by the monoclonal antibody 12G9 in Tetrahymena thermophila

We have employed monoclonal antibodies to reinvestigate the janus mutants of the ciliate Tetrahymena thermophila, which cause reversal of circumferential polarity on the dorsal surface of the cell. This reversal brings about frequent ectopic expression of ventral cortical landmarks, such as a "secondary" oral apparatus, on the dorsal surface. The principal antibody employed, FXXXIX-12G9, immunolabels both transient cortical structures not directly associated with basal bodies (the fission line and the postoral meridional filament) and more permanent structures (apical band and oral crescent) that are associated with basal bodies. 12G9-immunolabeling of janus cells has revealed additional phenotypes, including disorder of ciliary rows. Further, this labeling has shown that the postoral meridional filament is often expressed and the apical band is frequently interrupted on the mid-dorsal surface of janus cells irrespective of whether or not these cells express a "secondary" oral apparatus. Of the permanent structures revealed by 12G9 immunofluorescence, modifications of the oral crescent (OC) are associated with prior modifications in the development of basal body-containing structures in the secondary oral apparatus. The formation of the apical band (AB) is also commonly abnormal in janus cells; analysis of specific abnormalities shows that the AB depends both on its initiation at a specific site near the anterior basal body of apical basal body couplets and on the normal location of these couplets just posterior to the fission line. We also have uncovered an intriguing difference in the reactivity of apical-band filaments to the 12G9 antibody in the two non-allelic janus mutants (janA1 and janC2) that we have investigated. Taken together, our observations indicate that the formation of new cellular structures at division depends both upon pre-existing cytoskeletal structures and upon the positional information provided by large-scale cellular polarities.     

How the mirror-image pattern specified by a janus mutation of Tetrahymena thermophila comes to expression

The initial changes of cell-surface organization that occurred as the recessive janAl (janus) mutation of Tetrahymena thermophila first became expressed were elucidated in a special mating scheme in which old macronuclei homozygous for janA⁺ were synchronously replaced by new macronuclei homozygous for janAl. During this period of onset of expression, the number, regularity, and asymmetry of the ciliary rows remained unchanged. New normal (primary) oral apparatuses (OAs) continued to be formed posterior to old OAs, as in normal cells. At about four fissions after conjugation, abnormal (secondary) OAs with a partial reversal of asymmetry began to appear nearly opposite to the primary OAs, close to but not at the eventual circumferential position of janAl secondary OAs. The array of contractile vacuole pores (CVPs), normally located adjacent to two ciliary rows centered near 22% of the cell circumference to the righ of the primary oral meridian, underwent a two-step transformation: first, the number of adjacent ciliary rows bearing CVPs increased to 3, 4, and sometimes 5, then “skipped” rows appeared within this broadened CVP-arc to split the single set of CVPs into two separated subsets. The CVP transformations occurred gradually and progressively. They began prior to the expression of secondary OAs but accelerated as secondary OAs appeared. As the CVP are became broader, its midpoint shifted somewhat to the right, away from the primary oral meridian, but ended up close to halfway between the primary and secondary oral meridians. The data provide a better fit to an intercalation model than to an alternative double gradient model, suggesting that the janAl mutation alters the large-scale organization of positional values by preventing the expression of a subset of these values and thus provoking reverse-intercalation of the remainder.     

Morphology,Morphogenesis, and Molecular Phylogeny of Paraparentocirrus sibillinensis n. gen., n. sp., a “Stylonychine Oxytrichidae” (Ciliophora,Hypotrichida) Without Transverse Cirri

A terrestrial oxytrichid ciliate Paraparentocirrus sibillinensis n. gen., n. sp., which was found in soil samples of a beech forest stand within the National Park of Sibillini Mountains, Italy, was investigated using live observation and protargol impregnation. The morphology of interphase, morphogenesis, and molecular phylogeny inferred from SSU rDNA sequences of this ciliate were studied. Paraparentocirrus n. gen., is mainly characterized by a semirigid body, an undulating membrane in the Oxytricha pattern, six fronto‐ventral (FV) rows, the absence of transverse cirri, one right and one left row of marginal cirri, four dorsal kineties, two dorsomarginal rows, and caudal cirri at the end of dorsal kinety 4. During morphogenesis, oral primordia develop through the proliferation of basal bodies from some cirri of FV rows 4 and 5, and FV row 6 takes part in the anlagen formation of the proter. The dorsal morphogenesis was typical of oxytrichids, with simple fragmentation of dorsal kinety 3, and the dorsomarginal rows developed from the right marginal row. Phylogenetic analyses based on the SSU rDNA sequences support the classification of this new genus in the stylonychines.     

The oral apparatus of Tetrahymena pyriformis, strain WH-6. IV. Observations on the organization of microtubules and filaments in the isolated oral apparatus and the differential effect of potassium chloride on the stability of oral apparatus microtubules.

This report is an ultrastructural analysis of the organization of the isolated oral apparatus of Tetrahymena pyriformis, strain WH-6, syngen 1. Attention has been focused on the organization of microtubules and filaments in oral apparatus membranelles. Oral apparatus membranellar basal bodies were characterized with respect to structural differentiations at the distal and proximal ends. The distal region of membranellar basal bodies contains the basal plate, accessory microtubules and filaments. The proximal end contains a dense material from which emanate accessory microtubules and filaments. There are at least two possibly three different arrangements of accessory structures at the proximal end of membranellar basal bodies. All membranellar basal bodies appear to have a dense material at the proximal end from which filaments emanate. Some of these basal bodies have accessory microtubules and filaments emanating from this dense material. A possible third arrangement is represented by basal bodies which have lateral projections, from the proximal end, of accessory microtubules and filaments which constitute cross or peripheral connectives. There are at least three examples of direct associations between oral apparatus microtubules and filaments: (1) filaments which form links between basal body triplet microtubules, (2) filaments which link the material of the basal plate to internal basal body microtubules, (3) filaments which link together microtubule bundles from membranellar connectives. KCl extraction of the isolated oral apparatus resulted in the selective solubilization of oral apparatus basal bodies, remnants of ciliary axonemes and fused basal plates. Based on their response to KCl extraction two distinct sets of morphologically similar micro tubules can be identified: (a) microtubules which constitute the internal structure of basal bodies and ciliary axonemes, (b) microtubules which constitute the fiber connectives between basal bodies.     

Three new intestinal protozoan species of the genus Latteuria n.g. (Ciliophora: Trichostomatia) from Asian and African elephants

Three new ciliate species presumably belonging to the family Paraisotrichidae were recognized in the fecal samples from zoo-kept Asian and African elephants. All the ciliates possess a unique but similar arrangement of somatic ciliature, thus a new genus Latteuria n.g. has been created for them. The genus is characterized by the presence of a tapered frontal ‘spout’ at the anterior end of the body, posterior ciliary rows in narrow grooves encircling the posterior half of the body and an anterior arch of cilia. Latteuria polyfaria n.sp. is the largest species in the genus with 9–11 posterior ciliary rows. In L. media n.sp., of medium body size, the number of rows varies from four to six, and the smallest species, L. trifaria n.sp., has only three-four posterior ciliary rows.     

THE MORPHOGENESIS OF BASAL BODIES AND ACCESSORY STRUCTURES OF THE CORTEX OF THE CILIATED PROTOZOAN TETRAHYMENA PYRIFORMIS

Dividing cells of Tetrahymena pyriformis were observed by transmission electron microscopy for signs of morphogenesis of cortical structures. The earliest stage of basal body development observed was of a short cylinder of nine single tubules connected by an internal cartwheel structure. This is set perpendicular to the mature basal body at its anterior proximal surface under the transverse microtubules and next to the basal microtubules. Sequential stages show that the single tubules become triplet tubules and that the "probasal bodies" then elongate and tilt toward the organism's surface while maintaining a constant distance of 75–100 mµ with the "parent." The new basal body after it is fully extended contacts the pellicle, and then assumes a parallel orientation with and moves anterior to the parent basal body. The electron-opaque core in the lumen of the basal body and accessory structures around its outer proximal surface appear after the developing basal body has elongated. These accessory structures associating with their counterparts from other basal bodies and with the longitudinal microtubules may play a role in the final positioning of basal bodies and thus in the maintenance of cortical patterns. Observations on a second sequence of basal body formation suggest that the oral anlage arises by multiple duplication of somatic basal bodies.     

Different functions of tight junctions in the ascidian branchial basket

The stigmatal cells in the branchial basket of ascidians from a number of genera have been examined as to the nature and distribution of their intercellular junctions. The branchial wall consists of ciliated and parietal cells; the ciliated cells are arranged in seven rows and are associated by junctions with other cells in the same row as well as with those in adjacent rows. They are also associated by junctions with peripheral parietal cells. Junctions between adjacent ciliated cells in all cases exhibit tight junctions or zonulae occludentes. However, these cell borders also possess fasciae or zonulae adhaerentes if they are in the same row and the ciliary rootlets insert-into these junctions. If the cells are in adjacent rows they exhibit adhaerentes junctions only in species belonging to the orders Phlebobranchiata and Aplousobranchiata. In contrast, if the cells in adjacent rows belong to the order Stolidobranchiata. they never exhibit any adhaerentes junctions and the ciliary rootlets of the basal bodies from the cilia insert instead into the tight junctions and the non-junctional membrane below them. At the homologous junctional borders between adjacent parietal cells and also at heterologous junctional borders between parietal and ciliated cells, tight junctions alone occur, with no co-existing adhaerentes junctions along their lateral borders. Again, fibrils from ciliary rootlets insert into zonulae occludentes. This shows that tight junctions are capable both of forming permeability barriers, in that they can be seen to prevent the entry of exogenous tracers such as lanthanum, and of acting as adhesive devices.