Developmental control of lateralized neuron size in the nematode Caenorhabditis elegans
© Goldsmith et al; licensee BioMed Central Ltd. 2010
Received: 9 September 2010
Accepted: 1 December 2010
Published: 1 December 2010
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© Goldsmith et al; licensee BioMed Central Ltd. 2010
Received: 9 September 2010
Accepted: 1 December 2010
Published: 1 December 2010
Nervous systems are generally bilaterally symmetric on a gross structural and organizational level but are strongly lateralized (left/right asymmetric) on a functional level. It has been previously noted that in vertebrate nervous systems, symmetrically positioned, bilateral groups of neurons in functionally lateralized brain regions differ in the size of their soma. The genetic mechanisms that control these left/right asymmetric soma size differences are unknown. The nematode Caenorhabditis elegans offers the opportunity to study this question with single neuron resolution. A pair of chemosensory neurons (ASEL and ASER), which are bilaterally symmetric on several levels (projections, synaptic connectivity, gene expression patterns), are functionally lateralized in that they express distinct chemoreceptors and sense distinct chemosensory cues.
We describe here that ASEL and ASER also differ substantially in size (soma volume, axonal and dendritic diameter), a feature that is predicted to change the voltage conduction properties of the two sensory neurons. This difference in size is not dependent on sensory input or neuronal activity but developmentally programmed by a pathway of gene regulatory factors that also control left/right asymmetric chemoreceptor expression of the two ASE neurons. This regulatory pathway funnels via the DIE-1 Zn finger transcription factor into the left/right asymmetric distribution of nucleoli that contain the rRNA regulator Fibrillarin/FIB-1, a RNA methyltransferase implicated in the non-hereditary immune disease scleroderma, which we find to be essential to establish the size differences between ASEL and ASER.
Taken together, our findings reveal a remarkable conservation of the linkage of functional lateralization with size differences across phylogeny and provide the first insights into the developmentally programmed regulatory mechanisms that control neuron size lateralities.
One of the most fundamental aspects of biological control is the regulation of size, on the level of the individual cell, an organ, and the whole organism. Studies in yeast have yielded scores of genes controlling size, many associated with ribosomal protein synthesis . In metazoan organisms, growth and size control are usually studied on the level of either whole organs or even whole organisms, and several genetic mechanisms involved in organism and organ size control have been elucidated [1, 2]. For example, signaling pathways triggered by insulin and TGFβ are known to control organismal size [1–4]. Moreover, intriguing links between size control and tumor formation and suppression have been found in the form of genes such as Myc, Brat, and TFG[1, 2, 5, 6].
In spite of these advances, size regulation in the nervous system is poorly understood, even though the size differences of neurons are particularly astonishing. Cross-sectional cell soma size of neurons ranges widely from 0.005 mm to 0.1 mm in mammals. Size in terms of length of axon and dendrites can also hugely differ from neuron type to neuron type, from several microns to several meters within one given mammalian species. Two different nematode species, Caenorhabditis elegans and Ascaris suum have the same number and types of neurons (their axonal projection patterns are identical as well), yet they differ in soma size and neuronal processes length by several orders of magnitude . Even though the astounding range of neuron sizes in the nervous system has been known for a long time, few genes have been found that specifically control neuronal soma size. One striking case is the gene encoding the phosphatase PTEN, which, when knocked-out, results in a significant increase in neuron soma size, an effect mediated by the kinase mammalian target of rapamycin (mTOR) [8–10]. The importance of the PTEN-mediated neuron-size regulation is illustrated by Lhermitte-Duclos disease, which is characterized by overgrowth of neuronal soma [8, 9].
Neuron size regulation is particularly enigmatic when considering size difference between otherwise quite similar neuronal cell types. Such differential size regulation is strikingly apparent in one intriguing and poorly understood context in the nervous system, that of neuronal laterality. In general, nervous systems are morphologically bilaterally symmetric, yet they often are lateralized (left/right asymmetric) in specific functions . That is, groups of neurons located on one side of the brain perform different tasks than their mirror-symmetric neurons on the contralateral side of the brain. This lateralization is evident in many nervous systems across phylogeny, from worms to humans [11–14]. Yet how such asymmetry is genetically programmed is poorly understood. Curiously, in spite of the strong functional lateralization of many brain areas, there are very few genetic correlates to this asymmetry, that is, very few genes are known to be expressed in a left/right asymmetric manner in the adult nervous system of any species [12–14]. However, there is another quite striking correlate to functional asymmetry that has been described in several systems: a difference in soma size of contralateral neuronal ensembles. For example, within several subfields of the human hippocampus, there are regional differences in soma size in the left versus right hemisphere . Intriguingly, these hemispheric soma size differences are abrogated in schizophrenic patients . Left/right asymmetric soma size differences have also been observed within auditory and language-associated regions of the temporal lobe . Similarly, the optic tectum of birds, which is strongly functionally lateralized, displays soma size differences in contralateral neuron types [17, 18]. It is, however, not clear how widespread the coupling of functional lateralization and size regulation is. Also, virtually nothing is known about the underlying molecular pathways that control cell size in these left/right asymmetric, neuronal contexts.
Even though its neuronal anatomy has been described in detail, neuronal size has, somewhat curiously, not been studied at any great depth in C. elegans. Moreover, it has not been addressed whether functionally lateralized neuron pairs display soma size differences. If this were indeed the case, it may be possible to link genetic mechanisms that control functional lateralization to lateralized size control. We investigate this issue in this paper.
We visualized the ASEL and ASER gustatory neurons in live animals using chromosomally integrated gfp reporter gene constructs in which ASE-expressed cis-regulatory sequences drive non-localized green fluorescent protein (GFP), which diffuses throughout the entire cell and its processes (Figure 1A). Using two different transgenes (otIs242 = che-1 prom ::gfp and otIs125 = flp-6 prom ::gfp), we find that the two neuron soma show consistent and highly stereotyped size differences in adult animals (see Materials and methods for details on size measurements). The volume of the soma of ASER is more than 30% larger than the soma of ASEL (Figure 1).
We also examined a panel of additional neuron pairs in the head ganglia. We examined four additional sensory neuron pairs (AWCL/R, ADFL/R, AWBL/R, ASKL/R) and one interneuron pair (AIYL/R; the main postsynaptic target of ASEL/R). We found that even though there was some variation in individual animals, none of these neurons showed, on average, any indication of a consistent laterality in soma size (Figure 1C,D). This notion was corroborated by an analysis of sensory dendrite diameter, in which we also found no significant sidedness (Figure 3A), again in contrast to the situation with ASEL/R.
We examined the AWCL/R case in more detail. Like the ASEL/R gustatory neuron pair, this olfactory neuron pair is known to be functionally lateralized. The left versus right neurons sense different sensory cues and process information differentially [13, 24, 25]. However, in contrast to ASEL/R laterality, which is deterministic (that is, 100% invariant; a phenomenon called 'directional asymmetry') , AWCL/R asymmetry is stochastic (a phenomenon called 'antisymmetry') . This lateralization can be visualized with two distinct putative odorant receptors, str-2 and srsx-3. In 50% of animals str-2 is expressed in the AWCL, while in the other 50% it is expressed in AWCR. srsx-3 shows the complementary pattern. The str-2-expressing cell has traditionally been called the AWCon cell . Even though, on average, AWC soma showed no laterality, we tested whether the AWCon or AWCoff cell may correlate with a specific relative size. However, this is not the case (Figure 1C,D).
Taken together, the functionally lateralized ASEL/R neuron pair shows a consistent soma size laterality that is paralleled by axonal, dendritic, and nucleolar lateralities, but not by lateralities in nuclear size or DNA content. The neuron pairs that we examined for lateralities included neuron pairs in physical proximity to ASEL/R and/or related by common ancestry (that is, lineage). A lack of directional asymmetry in these related neuron pairs illustrates that it is not simply the case that one side ('hemisphere') of the worm is larger than the other, but rather that neuron size is regulated in a neuron-type-specific manner. We also note that absolute size measurements of other neuron pairs differ from neuron type to neuron type, with the larger ASER not being larger than other neuron pairs and the smaller ASEL not being smaller than yet other neuron pairs. It is therefore not obvious as to whether the size difference between ASEL and ASER is due to 'overgrowth' of ASER or 'growth inhibition' of ASEL.
To begin analyzing the genetic mechanisms that underlie these size differences, we first used a genetic background in which the ASEL/R neurons fail to be appropriately specified. The ASEL/R-specific che-1 Zn finger transcription factor is required for the correct development of ASEL/R neurons; in che-1 mutants, ASEL/R neurons are not functional (that is, animals are not able to chemotax to water-soluble attractants, hence the name che), and fail to express scores of genes that are normally expressed in ASE, yet the ASE neurons are still generated [20, 30, 31]. Measuring the size of ASE neurons in che-1 mutants, we find that the soma differences of ASEL and ASER are eliminated (Figure 5C). Left/right size differences are therefore programmed through the activity of the che-1 transcription factor.
We first analyzed ASE soma size lateralities in three different genetic contexts in which both neurons are transformed to the ASER fate ('2 ASER'; as assessed by gcy chemoreceptor gene expression). We used animals carrying loss-of-function mutations in the ASEL inducers die-1 (a Zn finger transcription factor) and lsy-6 (a miRNA), and transgenic animals in which the ASER-inducer cog-1 (a homeobox gene) is ectopically expressed in both ASE neurons. We find that in all three genetic backgrounds, both ASE neurons now adopt the larger size that is normally characteristic of ASER (Figure 6B). Similarly, we analyzed ASE soma size lateralities in two different genetic contexts in which both neurons are transformed to the ASEL fate ('2 ASEL'; as assessed by gcy chemoreceptor gene expression), namely in animals carrying loss of function mutation in the ASER inducers cog-1 and in transgenic animals that ectopically express the ASEL-inducer lsy-6 bilaterally in both ASE neurons. In both genetic backgrounds, both ASE neurons now adopt the smaller size that is normally characteristic of ASEL (Figure 6B). The effect of die-1 manifests itself not only on the soma size difference of ASEL/R, but also on difference in the number of nucleoli; they become bilaterally symmetric in the die-1 mutant (Figure 6C).
ASEL and ASER inducers act in a feedback loop . We sought to determine which genes provide the output from this loop to size control. For the determination of left/right asymmetric chemoreceptor expression, die-1 is the output, as the effect of die-1 on all previously known lateralities is epistatic to any genetic manipulations in the loop . We performed similar epistasis experiment, scoring asymmetric soma size. We find that die-1 is epistatic to both manipulations of cog-1 and lsy-6 activity (Figure 6B). That is, the '2 ASEL size' phenotype of either cog-1(-) or lsy-6 misexpression is reverted to the '2 ASER size' phenotype in a die-1(-) background.
The two transcription factors lim-6 (a LIM homeobox gene) and fozi-1 (a Zn finger transcription factor) act downstream of die-1 as effector genes, regulating a subset of left/right asymmetric features of ASEL and ASER (Figure 6A) [32, 33]. We find that these regulators have no impact on the ASEL/R soma size differential (Figure 6B).
Taken together, these findings show that size control is tightly controlled by a genetic regulatory mechanism that defines other aspects of laterality of the ASEL and ASER neurons as well. The control of left/right asymmetric size and chemoreceptor expression does, however, branch out downstream of die-1 (Figure 6A), as lim-6 and fozi-1 affect chemoreceptor expression but not size. We hypothesize that die-1 regulates either directly or indirectly the expression of effector genes that control size.
Background information on candidate genes tested for ASEL/R size differences
Reason for testing
Smad (TGFR signaling)
RBP (Brat tumor suppressor)
Controls cell size in C. elegans and other systems 
Insulin ligand a
Protein kinase B
Protein kinase B
Regulatory volume control in other systems
We found that reduction or elimination of only some of the candidate size regulators affect overall ASEL and ASER size (Figure 7A,B). These include the phosphatase PTEN, the kinase AKT, the Brat tumor suppressor Brat/Ncl-1 and the small GTPase Rheb-1, but surprisingly, not canonical size regulators, such as the insulin/IGF-1 receptor (Figure 7A,B). Of all the mutant animals tested, only one eliminated the difference in soma size between ASEL and ASER (Figure 7B). These animals carry a deletion allele, ok2527 (kindly provided by the Oklahoma C. elegans knockout consortium; Figure 7C) that eliminates the nucleolar protein Fibrillarin/FIB-1, an RNA methyltransferase involved in ribosome biogenesis . This finding is in accordance with the observation that ASER contains more FIB-1 positive nucleoli than ASEL (Figure 2). Linking FIB-1 accumulation to the upstream gene regulatory factors, we find that in die-1 mutants, the number of FIB-1(+) nucleoli increases in ASEL (Figure 6C).
Even though fib-1 is required for the manifestation of the size differences, it is not sufficient, as we did not observe any effect on the size differential in transgenic animals that overexpress fib-1 bilaterally in both ASEL and ASER using the ceh-36 promoter (four transgenic lines tested; data not shown). We also note that loss of fib-1 has no effect on left/right asymmetric chemoreceptor expression (gcy-5 and gcy-7; data not shown), corroborating the notion that size control can be decoupled from other aspects of ASEL/R laterality. In conclusion, our candidate gene analysis has uncovered a protein with a function in nucleolar biogenesis required for left/right differential size laterality in the nervous system.
We describe here a developmentally programmed size laterality of a functionally lateralized neuron pair. It is striking that the theme of lateralized soma sizes in functionally lateralized brain regions is conserved from higher vertebrates-for example, the optic tectum in chick [17, 18]-to a simple invertebrate like C. elegans.
The theoretical differences in passive voltage spread presented here (Figure 4) could have significant functional consequences. Other things being equal, one would expect stronger synaptic outputs from ASER in response to the same level of depolarization in the cilia of two neurons. Notably, it can be shown from first principles that for chemotaxis in a radial gradient, "off cells" like ASER (i.e. neurons responding to a decrease of a signal) are sufficient, whereas "on cells" like ASEL (i.e. neurons responding to an increase of a signal) are not . Thus, worms with stronger ASER outputs would enjoy a selective advantage, which may have resulted in an increase in ASER size. If validated experimentally, differential voltage spread would join a growing list of several distinct properties of the ASEL versus ASER neurons, including differential sensation of taste cues, differential chemoreceptor expression, differential response to upsteps (ASEL) versus downsteps (ASER) of chemosensory cues and differential contributions to spatial orientation behaviors [36, 38]. These features are layered upon otherwise largely symmetric characteristics of ASE . However, in contrast to the invariant left/right asymmetric expression of chemoreceptors, we note that the ASER > ASEL size differences are only observed when averaged over a population. That is, there are individuals in which either no differences in size are observed or in which the size asymmetry is reversed. Whether this is due to experimental error or is an indication of distinct chemosensory capacities of individual animals within a population remains to be determined.
fib-1 acts downstream, and is therefore a target of the die-1 Zn finger transcription factor, a conclusion based on our observation that the number of FIB-1(+) nucleoli increases - together with overall size - if normal die-1 expression in ASEL is lost. At this point, we can not tell whether the fib-1 locus is a direct transcriptional target of DIE-1 or whether differential FIB-1 accumulation in ASEL versus ASER is an indirect consequence of DIE-1 function in ASEL (or absence thereof in ASER). fib-1 is unlikely to be the sole (direct or indirect) target of DIE-1 in the context of size control since fib-1, unlike die-1, is not sufficient to impose ASER size. Work in yeast and flies has amply demonstrated that the genes encoding nucleolar proteins involved in ribosome biogenesis, such as fibrillarin, are co-regulated through common transcriptional control mechanisms ('Ribi regulon') [41–44]. Several distinct types of transcription factors are involved in controlling the Ribi regulon, such as the yeast Forkhead like protein Fhl1 or, in metazoans, the Myc transcription factor [42–44]. DIE-1 may either be directly involved in such a co-regulatory mechanism or may be involved in indirectly triggering such a mechanism via intermediary regulators (Figure 8). DIE-1 therefore joins the ever-growing list of transcriptional regulators of cell size; however, the role of DIE-1 in size regulation may be highly context dependent, as die-1 mutants do not display any gross defects in animal size.
Our analysis of candidate size regulators has also identified a series of genes that control overall neuron size in a bilaterally symmetric manner (that is, both ASEL and ASER are affected). Given the paucity of known size regulators in the nervous system, some of our partially unexpected results raise questions and provide a starting point for future analysis. As expected from work in other systems [8–10], daf-18/PTEN mutants show increased neuron size. However, a null mutation in the insulin/IGF-like receptor in worms, daf-2, does not affect neuron size, even though the same signaling system does have profound effects on size and growth in other organisms . Yet, loss of another gene in the daf-2 pathway, the Ser/Thr kinase akt-1 does significantly affect the size of both ASEL and ASER, suggesting that AKT may be coupled to a distinct upstream input. However, unlike in other systems, in which AKT negatively regulates size , ASEL and ASER size is increased in akt-1 mutants. A similar, unexpected 'sign reversal' is observed in animals lacking the size regulators rheb-1, a small GTPase, or the nucleolar protein nucleostemin/nst-1, both known to be required to promote growth in other systems [47, 48], but apparently inhibiting growth of both ASE neurons. Other known size regulators, such as cdk-4, do not effect ASEL/R neuron size at all. We also found no effect of removing the canonical size regulator let-363/ TOR; however, these animals could only be scored at the first larval stage due to later larval lethality. The maternal load of TOR may have rescued any potential size regulatory effect. The same caveat holds for interpretation of the lack of effect of removing let-60/ Ras and tfg-1/TFG. Lastly, we note that a transforming growth factor-β signaling pathway previously reported to control overall animal size in C. elegans does not affect ASE neuron size, demonstrating that overall animal size is decoupled from neuron size.
In conclusion, we have provided some of the first mechanistic insights into how lateralized neuron size is controlled and we have set a theoretic framework for the type of impact such size difference may have on neuron function. It is conceivable that lateralized neuron size differences in vertebrates may also be controlled via nucleolar mechanisms , a notion that is not a matter of course since known cell size control pathways do not necessarily work through regulation of ribosomal and hence nucleolar mechanisms . Our findings also raise the possibility that lateralized neuron size control may be uncoupled from more canonical mechanisms of size control in other cell and tissue types. This is because we find that asymmetric neuron size control is established at a stage (embryo) when no other tissues undergo the generic growth that is characteristic of late embryonic and larval growth and because asymmetric neuron size control does not involve many of the canonical body size regulators. The identification of direct target genes of the die-1 transcription factor, the regulator we found to impinge on the ASEL/R size differential, will provide more insights into this pathway in the future.
The following transgenes were used to measure neuron soma sizes: ASEL/R, otIs125 = flp-6 prom ::gfp; otIs242 = che-1 prom ::gfp; AWCL/R, otIs151 = ceh-36::dsRed2; AWCon/off, otEx9961 = srsx-3::TagRFP; AWCL/R, oyIs28 = odr-1::gfp; ADFL/R, zdIs13 = tph-1::gfp; AWBL/R, kyIs104 = str-1::gfp; ASKL/R, otEx4302 = sra-9::gfp; AIYL/R, otIs173 = ttx-3 prom ::gfp. ASE nuclear size was measured with otIs188 (che-1 fosmid ::yfp).
For the soma or nuclear size measurement, transgenic worms, harboring neuron-type specifically expressed reporter constructs are picked at the desired stage (either L1 or adult) and examined using an Axioplan 2 microscope and a Sensicam QE camera controlled by Micro-Manager software . Worms were rolled on the cover slip such that ASEL and ASER were in the same plane (dorso-ventral view), and stacks were made with a 63 × oil-immersion objective at 1 μm depth. The stacks were analyzed using ImageJ software, where the contrast of the cell was chosen such that the fluorescence intensity did not impinge on neighboring cells, and the ImageJ plugin Voxel Counter was used to count the number of pixels for each cell. GFP intensity was normalized by cropping stacks around each cell separately and adjusting the brightness levels of the two stacks such that the maximum intensity level of each stack was reset to one standard. Statistical analysis of the relative sizes within a given strain was also performed by using a paired two-tailed t-test; significance was determined using the Bonferroni correction. For sets of experiments where n ≥ 3, we employed the Bonferroni correction: instead of using thresholds of P < 0.05 or P < 0.01, we used stricter P-value thresholds of P < 1-((1-0.05)1/n) and P < 1-((1-0.01)1/n), respectively, where n is the number of experiments in a given set. We measured cross-sectional diameters in the electron micrographs by tracing each dendrite in ImageJ and using the Measure tool.
We measured ploidy by ethanol fixation followed by DAPI staining either otIs151 (ceh-36 prom ::rfp) or otIs232 (che-1::mChopti) for ASE cell identification. Image stacks of DAPI-stained worms were taken using the method described above. We measured DAPI intensity as a proxy for DNA amount and report the data as relative DAPI intensities. We used freeze fracture followed by methanol/acetone fixation for immunostaining.
To determine nucleoli size and number, we used cguIs001 (fib-1::gfp)  and an antibody against Nop1p (FIB-1) from EnCor BioTechnology (#MCA-38F3, Gainesville, FL, USA) at a 1:200 dilution, detected with a 1:200 dilution of an anti-mouse (Invitrogen #A-21202, Carlsbad, CA, USA") secondary antibody.
green fluorescent protein
insulin-like growth factor.
We thank Q Chen for expert assistance with generating transgenic lines, D Hall (Albert Einstein College of Medicine) for providing access to the archive of electron microscopical sections and help in data collection, the C. elegans knockout consortia for providing strains, SJ Lo for the fib-1 reporter, B Tursun for ASE reporters and members of the Hobert lab for comments on the manuscript. This work was funding by the NIH (5R03NS067451-02). OH is an Investigator of the Howard Hughes Medical Institute.
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