Plectus - a stepping stone in embryonic cell lineage evolution of nematodes
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Recent studies have challenged the widespread view that the pattern of embryogenesis found in Caenorhabditis elegans (clade 9) is characteristic of nematodes in general. To understand this still largely unexplored landscape of developmental events, we set out to examine more distantly related nematodes in detail for temporospatial differences in pattern formation and cell specification. Members of the genus Plectus (clade 6) seem to be suitable candidates to show variety, with certain idiosyncratic features during early development and the convenient availability of cultivatable species.
The study was conducted using 4-D lineage analysis, 3-D modeling of developing embryos and laser-induced ablation of individual blastomeres.
Detailed cell lineage studies of several Plectus species reveal that pattern formation and cell fate assignment differ markedly from C. elegans. Descendants of the first somatic founder cell S1 (AB) - but not the progeny of other founder cells - demonstrate extremely variable spatial arrangements illustrating that here distinct early cell-cell interactions between invariant partners, as found in C. elegans, cannot take place. Different from C. elegans, in Plectus alternative positional variations among early S1 blastomeres resulting in a ‘situs inversus’ pattern, nevertheless give rise to adults with normal left-right asymmetries. In addition, laser ablations of early blastomeres uncover inductions between variable cell partners.
Our results suggest that embryonic cell specification in Plectus is not correlated with cell lineage but with position. With this peculiarity, Plectus appears to occupy an intermediate position between basal nematodes displaying a variable early development and the C. elegans-like invariant pattern. We suggest that indeterminate pattern formation associated with late, position-dependent fate assignment represents a plesiomorphic character among nematodes predominant in certain basal clades but lost in derived clades. Thus, the behavior of S1 cells in Plectus can be considered an evolutionary relict in a transition phase between two different developmental strategies.
KeywordsNematode embryogenesis cell lineage cell specification evolution developmental system drift Plectus C. elegans
developmental system drift
embryonic growth medium.
The phylum Nematoda is considered a very ancient phylum reaching back into the Precambrian [1, 2, 3]. Well-preserved fossils of nematodes from the early Devonian very much resemble recent basal representatives . The number of extant nematode species is large with estimates ranging from tens of thousands to several millions [5, 6, 7, 8]. Their adaptation to nearly all environmental conditions would predict a high plasticity on the morphological and physiological level. But the nematode body plan has remained uniform, despite a high genetic divergence and evolutionary variations in core developmental pathways even between close relatives [9, 10, 11].
With respect to embryonic development, the strong similarities in cleavage pattern between the classic study object Ascaris megalocephala (today: Parascaris equorum; [12, 13]) and the modern model system Caenorhabditis elegans led to the notion that this represents how nematodes generally develop. Extended studies in representatives from different branches of the phylogenetic tree made clear, however, that despite strong conservation of morphology, their embryogenesis is surprisingly variable [7, 15, 16, 17] and hence the Ascaris/C. elegans pattern constitutes only one way to generate a worm.
Differences in early development among nematode species invalidate the long-standing notion formulated by von Baer  that during ontogeny first general characters are expressed that need to be conserved before evolutionary novelties are added.
Our recent analysis of basal nematodes (clades 1 and 2, according to the phylogenetic classification by  subdividing nematodes into 12 clades) revealed considerable differences from C. elegans, including lack of early asymmetric divisions associated with soma/germline separation, but also establishment of bilateral symmetry, spatial cell arrangements . Thus, nematodes appear to be an attractive taxon to study evolution of development.
Representatives particularly amenable for comparative embryonic studies should meet several criteria: simple culture conditions, fast development and transparent eggs. So far, only free-living members of clades 6 to 12 seem to fulfill these criteria . In search of candidates from these clades that may show developmental characteristics of both, basal nematodes (see above) and more derived species (clades 7 to 12; resembling the pattern found in Ascaris and C. elegans) representatives of the order Plectida (clade 6; ) appear to be promising candidates to search for such a combination of plesiomorphic and apomorphic characters. More than 70 different plectid species have been described  showing characteristic morphological features like setae (bristles) distributed over the entire body and unispiral amphids (chemosensory organs). The phylogenetic classification of plectid nematodes varied considerably in the past . Several members of the genus Plectus can be cultured in the laboratory and embryos are transparent enough with sufficiently rapid development to allow detailed lineage analysis . Among these, Plectus sambesii was found to have the fastest life cycle and highest reproductive rate under standard growth conditions. Therefore, most studies described here were performed on this representative, but other members of the genus were analyzed as well.
In the C. elegans embryo, cell specification requires reproducible spatial positioning of cells at specific milestone times to allow contacts and inductive signaling between neighboring blastomeres [23, 24, 25]. On the one hand, several plectid species were found to follow an early cleavage pattern similar to C. elegans, including the series of asymmetric cleavages going along with soma/germline separation. On other hand, plectids are clearly different in displaying an essentially perfect early bilateral symmetry within individual lineages and by initiating gastrulation prematurely with the immigration of an undivided gut founder cell .
In C. elegans, an invariant early left/right asymmetry is established in the 6-cell stage when two S1(AB) cell cousins on the left move anteriorly, while the corresponding pair on the right side moves posteriorly . As a result, cells occupying equivalent positions in the left and right branches of the lineage tree adopt nonequivalent fates, and, vice versa, equivalent cell fates in the left and right half of the embryo are executed in a complex manner by cells of nonequivalent position in the lineage . In the hatched worm, these early events result in a dextral handedness of organs. By experimentally inverting the left/right asymmetry of the four AB cells, a perfectly healthy ‘situs inversus’ (inverted left/right asymmetries) can be generated [27, 28]. As the left/right shift of early blastomeres, which in C. elegans is a necessary prerequisite for the typical pattern of inductive interactions, was not observed in Plectus, we wondered whether cell specification follows different rules in this genus. Therefore, we set out to compare cell lineages, spatial pattern formation and cell fate assignment in Plectus with those of C. elegans and representatives of basal clades in order to better understand the evolution of developmental processes during embryogenesis of nematodes.
Strains and culture
The strains Acrobeloides maximus (DF5048), Acrobeloides nanus (ES501), Aphelenchus avenae (RGD103), Bursaphelenchus xylophilus (S10), Caenorhabditis brenneri (SB280), Caenorhabditis briggsae (AF16), Caenorhabditis elegans (N2), Choriorhabditis dudichi (SB122), Diploscapter sp. (JU359), Diploscapter coronatus (PDL0010), Halicephalobus gingivalis (JB128), Panagrolaimus sp. (JU765), Panagrolaimus superbus (DF5050), Plectus aquatilis (PDL0018), Plectus minimus (PDL0012), Plectus sambesii (ES601), Plectus sp. (ES603), Pristionchus pacificus (PS312), Protorhabditis sp. (DF5055), Protorhabditis sp. (JB122), Rhabditis belari (ES103), Rhabditis dolichura (ES101), Teratocephalus lirellus (JB049), Tylocephalus sp. (PDL1001) and Zeldia punctata (PDL0003) were cultured at 23°C on minimal agar plates essentially as described in . Strains not isolated in our laboratory (ES) were obtained from Paul de Ley and Jim Baldwin, University of California at Riverside, USA; Marie-Anne Felix, Université Jacques Monod, Paris, France; Walter Sudhaus, Freie Universität Berlin, Germany; and Ralf Sommer, MPI for Developmental Biology, Tübingen, Germany. Data for Ascaris were taken from [12, 13], for P. marina from , and for H. gingivalis from . Recordings of Meloidogyne incognita were obtained from Bartel Vanholme and Alejandro Calderón-Urrea, California State University, Fresno, USA.
Cell nomenclature and cell fate assignments
Projection of C. elegans standard cell nomenclature [14, 31] onto other nematode species would imply similar cell fate patterns. Therefore, we apply neutral lineage names (S1to S4, somatic founder cells; P1 to P4, germline). In C. elegans, but not necessarily in other nematodes S1 = AB, S2 = EMS, S3 = C, S4 = D . For easier comparison between Plectus sambesii and C. elegans, we sometimes added for the former the standard names in parentheses.
Although we did not trace all embryonic divisions, we followed the behavior and localization of cells far enough to determine the tissues to which they contribute , in particular with respect to pharynx and hypodermis formation.
Early stage embryos collected from culture plates or cut out of gravid adults were mounted on slides carrying a thin 3% agarose layer as a mechanical cushion . Alternatively, gravid nematodes were dissected with a scalpel in a drop of distilled water on a poly-lysine-coated coverslip (0.01%) with a drop of petroleum jelly as spacer in all four corners (modified after ). The coverslip was sealed with melted petroleum jelly. Embryonic development was examined with DIC optics using a 100x objective. Stacks of optical sections were digitally recorded at 30 to 60 second intervals and at 23°C with a 4-D microscope. 3-D tracing of cell behavior and generation of cell lineages were software-supported (Simi Biocell, Unterschleissheim, Germany), originally described in . If not stated otherwise, development of at least seven embryos per species were analyzed.
Cell ablation experiments
1-cell embryos of P. sambesii were prepared for 4-D microscopy as mentioned above. For cell ablation, a Spectra-Physics Explorer™ Q-switched solid-state laser (Newport; Darmstadt, Germany) coupled to a Leica DMLB microscope (Leica; Wetzlar, Germany) via reflector optics was used. P1 and P2 cells were irradiated 3 × 45 seconds (at 50 Hz, 5 μJ) with 30-second intervals between irradiation periods. S3 cells were irradiated 3 x 30 seconds (at 50 Hz, 2 μJ) with 30-second intervals.
Cell extrusion experiments and cell culture
Manipulated embryos were cultured in embryonic growth medium (EGM) adopted from  to support closure of the vitelline membrane  necessary for normal development. Perforated embryos continued to develop to several hundred cells. In contrast to C. elegans, in P. sambesii this medium does not support differentiation of isolated blastomeres outside the protective vitelline membrane. 2-cell embryos of P. sambesii were mounted on poly-lysine-coated slides, and distilled water was then replaced by EGM. A hole was burned into the posterior part of the eggshell by pulsing repeatedly with the Spectra-Physics Explorer™ Q-switched solid-state laser (1 Hz, 60 μJ). By using gentle pressure with a needle on the coverslip, the P2 cell was squeezed out of the eggshell and detached from the remainder of the embryo . To visualize endocytotic activity as a marker for gut differentiation, EGM was supplemented with 0.25% Lucifer Yellow VS (LY, Mr 550, Sigma-Aldrich; Steinheim, Germany) and was allowed to penetrate the embryo by puncturing the eggshell with a laser microbeam . After 15 minutes’ incubation time, the LY medium was replaced by regular EGM. Localization of LY was visualized in terminal phenotypes by confocal microscopy.
Cleavage pattern in the P1 lineage is conserved between P. sambesii and C. elegans
Endoderm specification requires induction by P2
In C. elegans, gut (E) differentiation depends on an inductive signal between P2 (germline) and S2 (EMS) in a narrow time window in the early 4-cell embryo [39, 40]. Because of the differences in gastrulation (see introduction) we wondered whether in P. sambesii gut-specific differentiation depends on an induction by the germline, as found in C. elegans.
Since in C. elegans, physical separation of P2 in time from the remainder of the embryo reliably prevents gut induction [39, 40], we removed the germline blastomere in the early 4-cell stage through a laser-induced hole in the eggshell (n = 3; Figure3i). In these experiments, we added Lucifer Yellow to the extrusion medium, as this fluorescent marker dye is quickly and specifically taken up by gut precursor cells [38, 41]. In test experiments, we had determined that such an accumulation takes place in Plectus as well. After early P2 extrusion (n = 3), division of S2a and S2p was found to be essentially synchronous (Figure3m) in contrast to normal development. In addition, although the typical early immigration of the gut precursor cell took place, there was no accumulation of fluorescent dye in the descendants of this cell (Figure3j), indicating the absence of typical gut differentiation. To determine the time window of the assumed signaling, we then repeated this experiment in the late 6-cell stage after the division of the two S1 (AB) daughters (n = 2). Under these conditions, cell cycle lengths of S2a (MS) and S2p (E) became different from each other (Figure3l), normal internalization of S2p (E) took place, and fluorescent dye accumulated in the gut primordium (Figure3k).
Thus, our data show that, like in C. elegans, in P. sambesii: (i) P2 is necessary during the early phase of the S2p (E) cell cycle for proper endoderm specification and (ii) ablation of P2 is not sufficient to inhibit reliably its inductive signaling.
High positional variation of S1 cells in P. sambesii unlike in C. elegans
During embryonic development of C. elegans, but also P. sambesii (Figure1; ) pattern formation among P1 descendants takes place in a simple and invariant fashion. In contrast, in C. elegans, spatial arrangement of blastomeres and fate designation in the S1 (AB) lineage, even though invariant, is rather complex  and requires specific cell-cell interactions within narrow time windows [25, 39]. Based on our observation that pattern formation in the S1 lineage of Plectus differs from C. elegans, we started a more detailed 4-D analysis of embryonic S1 lineages in P. sambesii, including an evaluation of cell-cell contacts, spatial variations thereof and their effect on cell fate assignment (n = 73).
Hench et al.  reported recently that squeezing C. elegans embryos between microscope slide and coverslip can influence the spatial arrangement of blastomeres without necessarily compromising normal development. Therefore, we applied their minimal pressure-mounting technique for 30/73 embryos and for the remaining 43/73 embryos our standard procedure with an agarose pad as a cushion (see Methods). We found that the ratios of different spatial variants (described below) were not affected by the mounting technique applied.
During further development, three of the four above described polymorphs (Figure4a, m, s) were found to split into two further variants due to minor differences in orientation of certain cleavage spindles in the 16 S1-cell stage (Figure4d + d’, v + v’; corresponding variant of Figure4p not shown). Nevertheless, the general positions of the eight S1 cell clones relative to each other do not vary. While type R (a) and L (s) are frequent, the two variants of type M (g*, m*) are rare. In type L, the variants LR (n = 16) and LL (n = 12) occurred at about the same frequency, polymorph RL (n = 28) was twice as frequent as variant RR (n = 14). The rare types M2L (n = 1; Figure4p-r) and M2R (n = 1; not shown) occurred with the same low frequency. A corresponding equivalent to the single M1L variant (Figure4j-l) was not found in our collection.
Are polymorphic patterns genetically inherited?
As our studied P. sambesii strain reproduces parthenogenetically  and therefore genetic traits do not mix, we wondered whether the population is genetically diverse such that individuals with distinct developmental programs leading to one specific spatial pattern in their embryos coexist in fixed ratios.
To look for this, we recovered embryos whose early embryogenesis had been analyzed and allowed them to hatch and produce eggs. Samples consisting of multiple second-generation embryos from these single identified isolated mothers were noted and the eggs derived from each individual worm were studied to determine whether such eggs showed only the developmental pattern of their mother, or if one mother could produce different polymorphs. Among eggs from a mother of type M2R, we found 2 x LR, 2 x LL, 1 x RR, 4 x RL; in eggs from a mother of type LR we found 1 x LL, 2 x RR, 5 x RL; and in eggs from a mother of type RR, we found 4 x LR, 1 x LL, 1 x RR. These data demonstrate that in P. sambesii the different embryonic patterns are not inherited as exclusive genetic traits. Despite the small sample size, it appears likely that a mother can produce any and all of the observed polymorphs.
Differential behavior of S1 descendants depends on the P1 lineage
Our findings demonstrate that in the polymorphs of P. sambesii, cell positions and therefore cell-cell contacts of S1 descendants vary. This raises the question whether cell fate assignment in the S1 lineage can take place in the same way as in the monomorphic C. elegans in which a strict correlation with lineage origin exists  and specific inductions between individual cells are essential [23, 24, 25].
As earlier studies on another nematode, Acrobeloides nanus (clade 11), had shown an altered cleavage and differentiation pattern of S1 descendants after elimination of P1 [47, 48], we performed the same test with P. sambesii. After ablation of P1 (n = 11; Figure3a), the S1 descendants divide in a symmetric fashion and form a prominent blastocoel (Figure3b, c). No events resembling gastrulation (as we had found in A. nanus[47, 48] and R. culicivorax) were observed and the terminal phenotype did not show muscle contractions as found in experimental A. nanus embryos. However, with respect to cell cycle durations, manipulated Plectus embryos can be subdivided into two groups. In the first one (n = 5), descendants of S1 divided more or less synchronously (Figure3d) but, in contrast to the untreated embryo, the typical later retardation in parts of the S1 lineage was not found (see hypodermis specification below). In the second group (n = 6), early descendants of S1p behaved atypically in that they expressed retarded and differential cell cycles (Figure3e) while S1a descendants behaved normally. The retardation of S1 descendants (Figure3e) resembles that in the manipulated A. nanus embryos; however, a separation into AB and EMS fates (indicated by muscle contractions and gastrulation events) was not found. As our observations indicate an influence of P1 or its descendants on the behavior of S1 cells, we investigated to what extent specification of pharyngeal cells depends on inductions as in C. elegans.
Variable cell contacts indicate differences in specification of pharyngeal cells. In the monomorphic C. elegans, the pharynx is generated in a complex polyclonal way by a fixed subset of S1 (ABara and alp) and S2a (MS) descendants. Pharynx precursor cells enter the body cavity from the ventral side during late gastrulation forming a cylinder anterior of the intestine . Specification of S1-derived cells that contribute to the pharynx requires signaling from S2a descendants . We analyzed the situation in P. sambesii in order to explore to what extent cell specification in the detected polymorphs may differ from C. elegans.
Our cell lineage analysis revealed that the pharynx in P. sambesii is composed polyclonally of S1 (AB) and S2a (MS) descendants comparable to C. elegans. Only in the former, the extending blastopore forms a prominent furrow (Figure1h-j) through which pharynx precursors (descendants of S2a) are translocated into the center of the embryo. Cells on the margin of this furrow contributing to the pharynx belong to four of the eight S1 clones. However, their lineage origin varies in the R, M1, M2 and L polymorphs described above (Figure4, bottom). Hence, we conclude that in P. sambesii, the origin of the S1 contribution to the pharynx is not related to cell lineage origin and therefore must depend on cell position.
Specification of S1-derived hypodermis depends on cell position
In C. elegans the hypodermis of the hatching juvenile is generated in a reproducible manner by members of the S1 (AB) and S3 (C) lineages .
We revealed that in all observed polymorphs, only the S1 descendants in contact with S3 but not with P3 expressed a slower cell cycle (Figure6a1, c3-f3). To test whether this was due to an induction, we performed a series of cell ablation experiments.
After irradiation of S3 (n = 2) or their ancestors P1 (n = 3) and P2 (n = 3), the typical retardation of posterior S1 descendants did not take place (Figure3q) and no cells with hypodermis-like characteristics (see Methods) formed. In contrast, normal formation of hypodermis took place after ablation of S2a (data not shown). Hence, our results indicate that specification of hypodermis from variable posterior S1 cells takes place in a position-dependent manner and involves signaling by S3.
Variable chirality during early cleavage but invariant handedness of adults indicates position-dependent cell specification
All specimens showed the standard left-right asymmetries (Figure7f) and not a single situs inversus was detected. This allows the conclusion that in the P. sambesii embryo, all of the identified polymorphic variants merge into a single adult phenotype. This finding gives further support to the conclusion drawn from the other observations reported above, that is, that in contrast to C. elegans, cell specification of S1 descendants depends on position in the embryo rather than position in the lineage tree.
A shift from polymorphic to monomorphic embryogenesis supports a subdivision of the taxon Chromadorea
Studies in other representatives of clades 8 and 9, for instance D. coronatus, P. marina or C. briggsae, revealed that these are monomorphic and that development is very similar to that of C. elegans.
The results from this comparative study support a subdivision of the taxon Chromadorea  into species with a Caenorhabditis-like development (‘Rhabditia’) and those following a Plectus-like development (‘Chromadoria’). Such a separation had been suggested earlier based on morphological and developmental peculiarities in clades 3 to 6 [7, 22, 51].
Nematodes of clade 6 appear to follow a different developmental strategy
The study of embryogenesis in 28 nematode species from clades 6 to 12 (according to the phylogeny of ) representing different early cleavage patterns demonstrates a high diversity during early development and indicates major evolutionary modifications in the early cleavage and differentiation program of nematodes . Surprisingly, embryogenesis in all 23 species of clades 7 to 12 merges into a common monomorphic (invariant) cell pattern prior to the onset of gastrulation comparable to that described for Ascaris[12, 13, 52] and C. elegans[14, 31]. The conserved spatial pattern following the initial variant phase can be best explained with the necessity for specific cell neighborhoods to allow inductions essential for proper specification of blastomeres . Initially, founder cells need to be positioned in a specific order along the primary body axis [14, 17], then orientation of subsequent cleavages, steric constraints and secondary early cell rearrangements  result in a common monomorphic pattern.
However, our findings in Plectus sambesii and other representatives of clade 6 with their variable cell localization of S1 descendants appear to reflect a different developmental strategy. These species pass through a polymorphic development with a limited number of spatial variants, which nevertheless result in a single adult phenotype. This excludes a lineage-dependent early cell-specification as found in C. elegans[14, 25] and gives no indication for a global cell sorting as postulated by Schnabel et al. .
Embryonic cell patterns and establishment of left/right asymmetry
In many bilaterian animals, a left/right asymmetry of their internal organs has been found whereby one variant of asymmetry is predominant while the other (‘situs inversus’) is rare or even absent [54, 55]. In a variety of nematode species, a preferred handedness was reported by zur Strassen  and explained with Mendelian inheritance. In Ascaris as well as in C. elegans, this asymmetry is established already in the 6-cell stage embryo when a shift of the left pair of AB cell cousins relative to their counterpart on the right side takes place [12, 26, 56]. In all analyzed species of clades 7 to 12 (Figure8) we observed only right-handed embryonic asymmetry resulting in a single corresponding adult phenotype. As an experimentally induced inverted embryonic asymmetry in C. elegans results in healthy, fertile ‘situs-inversus’ adults [27, 28], the dominance of one variant is obviously not due to a developmental necessity but may have been fixed in the population because of steric or genetic constraints  or later benefits, like increased mating success as suggested by zur Strassen . So far, only one nematode species has been described where a sinistral embryonic and adult phenotype is standard  but studies in other systems, such as snails and mice, indicate that a switch in handedness can be induced by a single mutation [58, 59]. In contrast to the nematodes mentioned above, in Plectus sambesii we not only identified left and right but also rare intermediate embryonic patterns, which, however, all lead to the same dextral adult phenotype (Figures 4,7). The unusual variation in the arrangement of coherent clonal regions exhibited by plectids with their implications on cell specification invokes the question of what changes must have taken place during evolution to come from a polymorphic, Plectus-like to a monomorphic, C. elegans-like mode of development and what the driving forces for this may have been.
Evolution of cell lineage and cell specification - a scenario
In a recent publication , we sketched the gradual evolution from basal nematodes of the taxon Enoplida (clade 1) with no detectable early cell lineage  and delayed fixation of cell fate  via representatives with a partial early lineage as found in Tobrilus to Romanomermis (clade 2) with invariable development but predominantly monoclonal lineages. For a better understanding of how evolution proceeded to species with a complex polyclonal lineage as found in C. elegans and all other studied representatives of clades 7 to 12 [29, 50, 61] our findings in Plectus may be helpful.
Taking for granted that each taxon exhibits a combination of plesiomorphic and apomorphic characters, Plectus can be viewed as a stepping stone between basal nematodes (clades 1 to 2) where early specification is absent  and more derived representatives (clades 7 to 12; see Figure8) with their invariant, polyclonal cell lineage. While in Plectus the descendants of P1 behave invariantly, this is markedly different in the progeny of S1 (AB). However, the variants in this lineage do not show a random distribution. The dextral-type RL is by far the most abundant (Figure4) and this is just the one and only variant present in C. elegans, suggesting that, on an evolutionary time scale, Plectus may be on its way toward an invariant cleavage pattern as found in C. elegans.
We envision four important steps for such a transition to happen. (i) Starting from a nematode with a polymorphic monoclonal cell lineage (so far hypothetical), the introduction of position-dependent inductions initiates the beginning of a polyclonal lineage whose complexity will increase over time. (ii) The initially random distribution of polymorphic variants becomes biased, possibly by steric constraints like changes in shape or size of the eggshell or modified orientation of cleavages. The observed predominance of dextral variants in Plectus (Figure4) may serve as an example for this. Compared to Plectus (Figure1; ), the C. elegans embryo is more jammed inside the egg envelope, giving a possible explanation for an increase of situs inversus there after removal of the eggshell . (iii) The essentially perfect bilateral symmetry as found in Romanomermis[16, 32] and Plectus (Figures 2,6; ) is broken and compensated by inductions [23, 24, 25] resulting in cells that perform equivalent fates in the left and right half of the embryo, although they occupy nonequivalent positions in the lineage tree. A variety of such examples can be found in the AB lineage of C. elegans. (iv) The genetic fixation of cell fate via signaling of neighboring cells reduces tolerable variability and eventually leads to a monomorphic pattern. This goes along with an increasingly earlier specification of blastomeres. Elimination of gene function (see http://www.wormbase.org) and cell isolation experiments [63, 64] demonstrate the presence of a tightly woven network of early cell-cell interactions in C. elegans.
Lineage versus position. How big is the difference between Plectus and C. elegans?
The highly variable patterns of S1 cells in Plectus demonstrate the requirement of cell-cell interactions for proper cell specification. How fundamental then is the difference to C. elegans? The classic view of a purely cell-autonomous intrinsic cell specification in nematodes [42, 65] has been overcome with the discovery of early cell-cell interactions in C. elegans (for recent review, see ) which include S1 cells. A strong argument that in C. elegans fate assignment in the S1 lineage must also depend on extrinsic inductions beyond the cases revealed so far is supplied by the finding that an isolated S1 cell generates only surviving descendants that contribute to the nervous system when cell-cell signaling is suppressed [45, 67]. Promising candidates for further inductions in the S1 lineage include, for instance, anterior descendants with equivalent positions in the left and right half of the embryo but nonequivalent lineage affiliation, which nevertheless execute equivalent, bilateral symmetric fates . Thus, the prominent difference between both species with respect to cell specification of S1 cells can be considered a gradual and not a fundamental one. The variable pattern formation going along with late, position-dependent fate assignment as found in Plectus appears to be a plesiomorphic character predominant in certain basal nematodes but lost in representatives of clades 7 to 12. In this respect, Plectus and its kin may be in a transition phase between two different developmental strategies.
Evolution of cell lineages and gene regulatory networks
The driving forces for the establishment of a C. elegans-like cell lineage mechanism could be a faster developmental tempo due to an increased recourse to maternal gene products, an improved cost-efficiency of embryogenesis  or a better reliability of the cell-specification program, resulting in higher reproductive success. It has been argued that a monoclonal lineage allows a simple way for cell specification but requires extensive cell migrations, whereas a polyclonal lineage means more cell specification decisions but allows cells to be born where they are needed [29, 69]. Both strategies have their advantages, but when rapid development and low cell numbers are an issue, a polyclonal invariant development should be superior. In addition, subdivision of a lineage into many small modules offers increased options for evolutionary fine-tuning. Thus, a polyclonal lineage offers more flexibility in the course of phylogeny, but less during ontogeny .
Studies on embryonic cell specification  vulva formation [11, 70] and sex determination  in nematodes of the same clade as C. elegans revealed major modifications with respect to the underlying gene regulatory networks. Changes in the subcellular control mechanisms of development without corresponding reflections on the anatomical level, called developmental system drift , appear to be a common process in the animal kingdom, indicating that selective pressure is low on how to make an organism, but high on the functional capability of the final product. The cellular variations we report here together with previous studies [7, 17, 32, 73] suggest that even more significant alterations of the molecular machinery can be expected when representatives of the whole phylum are compared. Initial support for this comes from genomic and gene expression data of various nematode species ([74, 75]; our unpublished results). Nematode embryogenesis taking place in the protected encasement of a rigid egg envelope appears to be a fertile field for the exploration of alternative developmental pathways.
Our embryonic studies in nematodes of the genus Plectus reveal major differences with C. elegans. Most prominent is the variable positioning of S1 (AB) descendants, implying a position- rather than lineage-dependent mode of cell specification. With this peculiarity, Plectus appears to occupy an intermediate position between basal nematodes following an indeterminate early development and the C. elegans-like invariant pattern. Our results exemplify that developmental system drift not only allows large-scale modifications of gene regulatory pathways without impact on morphology but also of blastomere behavior during embryogenesis. While nematodes seem to be particularly suitable for studying the evolution of development due to their long history, ubiquitous distribution and amenability for detailed lineage analysis, the challenge for the future will be to correlate the alteration of cell behavior with the dynamics of the underlying molecular scaffolding.
We are indebted to various colleagues for sharing strains (listed in Methods) and to Oleksandr Holovachov for identification of P. cf. sambesii. We appreciate the critical reading of the manuscript by Randy Cassada and Curtis Loer. JS was supported by the Deutsche Forschungsgemeinschaft (Schi 214/16-1); WH was supported by the Foundation of Scientific Research, Flanders (FWO, grant number 1.5.122.08 N).
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