Abstract

Introduction

During metazoan development, cell division and cell differentiation must be spatially and temporally coordinated in order to generate the correct quantity and quality of cells in the right place at the right time. Since the timing of cell division is ultimately controlled by the conserved cell cycle machinery, understanding how the cell cycle influences cellular differentiation programs and, conversely, how developmental decisions feed into the regulation of cell cycle machinery is a fundamental challenge of developmental biology.

Cyclin-dependent kinases (CDK) associate with specific regulatory subunits called cyclins to drive cell cycle progression.¹ Cyclins, as the name implies, oscillate through the cell cycle and impart to CDK substrate specificity that is appropriate to the particular cell cycle phase. CDK1 and cyclin B form the archetypical CDK/cyclin complex known as mitotic (M)-phase-promoting factor (MPF), which is essential for mitotic and meiotic cell cycle progression.¹ CDK2 and cyclin E, on the other hand, mediate the entry of cells into the DNA synthesis (S) phase and the expression of S-phase-specific genes.⁴ Some animal genomes encode an extensive repertoire of CDKs and cyclins. For example, the human genome encodes more than 20 CDK genes and more than 10 cyclin genes.^2,3 With the expansion of the CDK and cyclin families, the roles they play have also expanded to include diverse functions in transcription, signal transduction, epigenetic regulation, metabolism, stem cell self-renewal, neuronal functions, and spermatogenesis.³

Two recurrent themes in development that demand coordination between the cell cycle and differentiation programs are asymmetric (or unequal) cell division and the maintenance of cell-proliferation zones. Asymmetric cell division occurs when a cell divides to generate 2 daughter cells that are committed to different cell fates. Molecular mechanisms governing this process have been studied extensively from yeast to multicellular organisms.^5-9 During asymmetric cell division, cells appear to become polarized in response to an intrinsic cue, or in response extrinsic signals from neighboring cells. The generation of daughter cells with distinct developmental fates then requires that the mitotic apparatus orient itself such that the polarized contents of the cell are partitioned unequally to the daughters. We will discuss recent studies that suggest how the core cell cycle machinery may coordinate this process to ensure proper cell division orientation and timing. Another major theme in development is the maintenance of cell-proliferation zones essential for growth, organ homeostasis, and stem-cell renewal. Recently, new insights into how a variety of proliferation signals modulate core cell cycle factors are beginning to shed light on this fascinating process. The studies reviewed here elucidate the developmental roles of CDKs and cyclins and provide insights into how developmental decisions may be coupled with cell cycle regulation.

CDK1 and Cyclin E in Asymmetric Cell Division in Flies

One of the first examples of CDK1’s role in differentiation came from the studies of asymmetric cell division of neuroblasts in the central nervous system of the fruit fly.¹⁰ Fly neuroblasts undergo multiple rounds of asymmetric cell division along the apical/basal axis to produce the neurons that populate the central nervous system. Each asymmetric division produces a larger apical cell that retains neuroblast (NB) identity and a smaller basal cell, called the ganglion mother cell (GMC), which divides once giving rise to 2 cells with neuronal or glial identity (Fig. 1A).¹¹ A set of conserved apical and basal proteins function to set up a polarity along the apico-basal axis of the neuroblast and cause the basal cell fate determinants Prospero and Numb to asymmetrically localize on the basal cortex as crescents during neuroblast cytokinesis. The asymmetric distribution of cell fate determinants and alignment of the mitotic spindle along the apico–basal axis ensures that the basal cell fate will be induced in each basal daughter cell. Mutations that perturb the asymmetric localization or function of the basal cell fate determinants result in symmetric neuroblast division and fate-specification defects of its daughter cells.^5,7,9

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Figure 1. (A) Asymmetric segregation of cell fate determinants in asymmetric neuroblast cell division of Drosophila. Apical factors (such as Insecutable and Pins, and the evolutionary conserved Par complex consisting of Par-6, Bazooka, and Cdc42) shown in blue and basal factors (such as Miranda, Prospero, and Numb) shown in red are asymmetrically localized on the cortex along the apico–basal axis of neuroblast (left) and segregated asymmetrically to larger apical cell that retains neuroblast (NB) fate and smaller basal cell called ganglion mother cell (GMC). Mitotic spindle that orients along the apico–basal axis ensures asymmetric inheritance of the cortical cell fate determinants. Cdc2 activity is required to maintain the cortical asymmetry during cell division. (B) Asymmetric cell division of thoracic neuroblast 6-4 (NB6-4). NB6-4t divides asymmetrically to produce a neuroblast (blue) and gliablast (orange), whereas NB6-4a divides symmetrically giving rise to 2 glial cells. The neuroblast identity is maintained by high levels of Cyclin E (white stars), which is significantly reduced in NB6-4a.

A genetic screen for mutants with defects in the asymmetric localization of apical and basal proteins in neuroblasts identified a hypomorphic missense mutation of CDC2 (CDK1), cdc2^E51Q, suggesting the involvement of CDC2 activity in the neuroblast asymmetric cell division.¹⁰ In the mutant neuroblast, apical factors such as Inscuteable and Bazooka, as well as basal factors such as Prospero, Pon, and Miranda are all mislocalized, and the mitotic spindle fails to orient along the apico–basal axis of the cell. Detailed analyses using a temperature-sensitive allele of cdc2 as well as rescue experiments using wild-type and kinase-dead alleles of cdc2 demonstrated that the kinase activity of CDC2 is required for the asymmetric cell division of neuroblasts, and that attenuation of CDC2 activity results in the loss of the neuroblast asymmetric cell division without hindering mitosis. Temperature-shift experiments using the temperature-sensitive allele of cdc2 suggested that CDC2 activity is required for maintaining the asymmetric localization of apical complex proteins during mitosis but not for the initial establishment of asymmetry during interphase. Furthermore, genetic studies revealed that anaphase-specific cyclins, namely Cyclin B and Cyclin B3, but not metaphase-specific Cyclin A, are involved in maintaining the asymmetry of apical proteins. These results suggest that the kinase activity of CDK1/Cyclin B complex is specifically required for maintaining the apico–basal polarity of neuroblasts during mitosis.

Individual neuroblasts produced from corresponding positions in thoracic and abdominal segments usually acquire similar fates in the developing fruit fly. However, the neuroblast NB6-4 lineage is a case where variations exist.¹² In the thoracic segments of the embryonic central nervous system (CNS), NB6-4t divides asymmetrically to generate one neuronal and one glial precursor cell. The neuronal precursor cell then divides several times in stem-cell mode to generate a neuronal sublineage. The glial precursor cell, however, divides twice to generate 3 glial cells. In the abdominal segment of the embryonic CNS, the corresponding neuroblast (NB6-4a) merely divides symmetrically into 2 glial cells (Fig. 1B). Mutations in homeotic genes abd-A and abd-B cause abdominal NB6-4 to transform into the more elaborate thoracic lineage. Conversely, overexpression of abd-A results in the opposite NB6-4t to NB6-4a transformation.¹³ Genetic and biochemical evidence demonstrate that these homeotic transformations are dependent on Cyclin E. In Cyclin E loss-of-function mutants, thoracic NB6-4 adopts the fate of its abdominal counterpart, generating only 2 glial cells. Conversely, ectopic expression of Cyclin E in abdominal NB6-4 transforms its mode of division to one that resembles thoracic NB6-4. In situ hybridization reveals that Cyclin E is expressed in thoracic NB6-4 but not in the abdominal counterpart (Fig. 1B). After the first asymmetric division, Cyclin E mRNA is detected in the neuronal precursor but not in the glial precursor daughter cell. In abd-A mutant embryos, which exhibit an abdominal-to-thoracic NB6-4 transformation, Cyclin E mRNA is detected in the transformed NB6-4a lineages. Importantly, overexpression of abd-A, which causes the opposite transformation, reduces Cyclin E mRNA levels in the thoracic segment. Perhaps most critical, the homeotic transformation observed in abd-A mutants is suppressed by mutations in Cyclin E. This epistatic evidence, along with potential Abd-A-binding sites in the Cyclin E promoter, suggest that homeotic genes in the Bithorax complex regulate the differential expression of Cyclin E, which maintains the neuroblast stem cell fate.¹³ Interestingly, Cyclin E co-precipitates with Prospero, suggesting that it may play a role in the asymmetric localization of a key basal fate determinant.¹⁴

An alternative mode by which Cyclin E regulates differentiation has been described in Drosophila female germline stem cells.¹⁵ Germline stem cells in mosaic germaria carrying partial loss-of-function alleles of Cyclin E or Cdk2 display normal rates of proliferation as long as they are within the stem cell niche, reflecting that the cell cycle machinery is still intact. However, these CDK2/Cyclin E compromised germ cells fail to maintain their proliferative fate due to a weakened response to niche bone morphogenetic protein (BMP) signals. BMP ligands expressed in the niche are required for germ stem cell maintenance. Reduced levels of pMad (a reporter of BMP signaling) show that Cyclin E mutant GSC do not respond properly. As a result, germ cells are lost from the stem cell niche, arrest in the G₁ stage of the cell cycle, and grow excessively without differentiating. This impaired response to BMP induction suggests that CDK2 and Cyclin E maintain germline stem cells by modulating the response to niche-derived signals.

Cell Fate Specification Regulated by C. elegans CDK1

The C. elegans zygote undergoes 5 rounds of successive asymmetric cell divisions, through which 5 somatic founder cells and 1 germline cell are produced. Mutations that perturb these asymmetric cell divisions are easily recognizable due to the absence of specific tissues and/or the presence of extra tissues, reflecting the misspecification of founder cell fates. cdk-1(ne236) and cdk-1(ne2257) are 2 hypomorphic alleles of C. elegans CDK1 that were initially identified in forward genetic screens for embryonic lethal mutations exhibiting defects in cell fate specification.¹⁶ These 2 unique alleles of CDK1, one non-conditional (ne236) and one temperature-sensitive (ne2257), exhibited essentially an identical phenotype, in which the founder cell “C” produces extra intestinal tissue instead of giving rise to hypodermis and body wall muscle. cdk-1 is essential for cell division.^17,18 However, the phenotypes exhibited by these mutants were not simply caused by defects in cell cycle progression; for both mutants, the striking defects observed in cell fate specification occur in embryos that show an otherwise wild-type pattern and timing of cell division.¹⁶ Consistent with these findings, when immunoprecipitated from embryonic lysates CDK-1(ne2257) was shown to phosphorylate Histone H1, a well-known CDK1 substrate during mitosis, at levels similar to that observed for wild-type CDK-1.¹⁶ These observations suggest that the function of cdk-1 in cell fate specification can be uncoupled from its role in driving progression through the cell cycle.

Structural basis of the peculiar phenotype exhibited by cdk-1(ne2257 and ne236) was suggested from the examination of the crystal structure of the activated mouse CDK2/Cyclin A complex.¹⁹ The T-loop of CDK2, which harbors the mutations found in ne2257 (I173F) and ne236 (R176H) (Fig. 2A), resides at the interface of CDK2 and Cyclin A subunits of the activated kinase complex, suggesting that amino acid substitution therein could have a subtle effect on cyclin binding (Fig. 2B). For example, the amino acid affected in cdk-1(ne2257), Ile-173, is positioned in the co-crystal structure in very close proximity to Ile-114 of CYB-3 (Cyclin B3 in C.elegans). Perhaps accommodating the bulkier amino acid, phenylalanine, as found in cdk-1(ne2257), alters the conformation of the active kinase complex sufficiently to perturb substrate-recognition interactions important for the cell fate specification without preventing interactions important for cell cycle progression. Consistent with this idea, a screen for mutants that can suppress the embryonic lethality of cdk-1(ne2257), identified a compensatory mutation in which Ile-114 of CYB-3 is changed to a much smaller amino acid, valine (T.I. and C.M., unpublished results).

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Figure 2. (A) Alignment of amino acid sequences surrounding the T-loop region of CDK1 from worm, fly, and mouse, showing the positions of conserved amino acid sequence mutated in the hypomorphic alleles of cdk-1 (ne2257 [I173F] and ne236 [R176H]) isolated in genetic screens using C.elegans, boxed in red or yellow, respectively. Invariant amino acids are indicated with an asterisk. (B) Crystal structure of activated mouse CDK2/CyclinA complex. Amino acids corresponding to those affected in the hypomorphic alleles of cdk-1, Ile173 in the case of ne2257, and Arg176 in the case of ne236 are shown in red and yellow, respectively. The amino acids corresponding to those affected in 2 cyb-3 suppressor alleles of cdk-1(ne2257) are also shown in magenta (ne4276) and light blue (ne4277).

Detailed genetic and biochemical analysis of the phenotypes caused by these subtle mutations in cdk-1 has uncovered at least 2 biological contexts in which cell cycle-independent functions of CDK-1 contribute to the asymmetric inheritance of cell fate determinants during early embryogenesis. In the first of these, CDK-1 plays a role in the transition from oocyte to embryo by timing the elimination of the OMA-1 protein after the first cell division. In the second, CDK-1 activity couples the orientation of the cell-division axis of the EMS blastomere with a polarizing signal in the 4-cell stage embryo.

CDK-1 regulates the transition from oocyte to embryo in C.elegans

The first evidence linking cdk-1 to the asymmetric localization of cell fate determinants came from the realization that the cell fate transformation observed in cdk-1(ne2257 and ne236) was essentially identical to that seen in a gain-of-function mutation of oma-1(zu405). OMA-1, and its closely related homolog OMA-2, are CCCH-type zinc-finger proteins expressed in oocytes and zygote and required redundantly for oocyte maturation.^20,21 A study using GFP-tagged OMA-1 protein revealed that while OMA-1 protein resides uniformly throughout the cytoplasm during oogenesis and in early one-cell stage embryo, it undergoes an abrupt degradation during the first mitotic cell division. OMA-1 protein level is further reduced during the second division, after which it becomes almost non-detectable at the 4-cell stage.²² Interestingly, in the gain-of-function oma-1(zu405) mutant, as well as in cdk-1(ne2257 and ne236), OMA-1 degradation fails to occur, causing OMA-1 protein to persist beyond the 4-cell stage. Reduction of OMA-1 protein level by loss-of-function mutations or by RNAi rescued the embryonic lethal phenotype of oma-1(zu405) and, importantly, also rescued the cell fate transformation and lethality of cdk-1(ne2257). Further genetic studies implicated cyclin B3 but not cyclin A in the regulation of OMA-1 stability.¹⁶ Thus, a CDK-1/cyclin B3 complex promotes OMA-1 protein degradation during the first cell cycle to ensure proper cell fate specification in the initial asymmetric cell divisions of the C. elegans embryo.

Recent studies have elegantly demonstrated that the OMA proteins are multi-functional repressors that prevent the premature activation of developmental gene expression in oocytes and early embryos, and that they achieve this regulation through both transcriptional and translational repression.^23,24 First, in the zygote as well as in the germline cell in the 2-cell stage embryo, the OMA proteins repress the RNA polymerase II complex (TFIID) by binding to and sequestering TAF-4, an essential component of TFIID.²³ Second, in 2-cell and 4-cell embryos the OMA proteins directly bind the 3′ UTR and inhibit the translation of ZIF-1, a substrate-binding subunit of a CUL-2-containing E3-ubiquitin ligase that degrades PIE-1.²⁴ PIE-1 is a CCCH homolog of OMA-1 and like OMA-1 appears to function as a global repressor of transcription in the germline.^25,26 Thus, persistence of OMA-1 leads to loss of PIE-1 function, which, in turn, leads to de-repression of SKN-1, the master regulator of intestinal development, leading, among other defects, to the ectopic production of intestine by descendants of the 4-cell stage germline blastomere, P2.

Forward and reverse genetic approaches have revealed that cdk-1 is only one piece of a multi-step mechanism that promotes the timely degradation of OMA-1 at the transition from oogenesis to embryogenesis (Fig. 3A).¹⁶ A set of biochemical experiments revealed that OMA-1 degradation is promoted by a series of sequential phosphorylations, initiated by a DYRK family kinase MBK-2, a kinase known to phosphorylate various substrates during oocyte-to-embryo transition, marking them for ubiquitin-mediated protein degradation pathway. The phosphorylation of OMA-1 by MBK-2, in turn, serves as the priming phosphorylation for subsequent direct phosphorylations by GSK-3 and Casein Kinase 1, all of which are required for OMA-1 degradation.^16,27,28 In addition, MBK-2 phosphorylation promotes the dissociation of OMA-1 from SPN-2 and its interaction with TAF-4,^23,24 providing a striking example of how regulations of multiple independent functions and activities of a protein can be coupled. Activation of MBK-2 itself is subject to multi-layered regulation that includes phosphorylation by CDK-1 during oocyte maturation, as well as dynamic regulation of its subcellular localization from the cortex to cytoplasm involving the protein-tyrosine phosphatase-like proteins EGG-3/4/5 that tether MBK-2 to the cortex (Fig. 3A).^29,30 Thus CDK-1 contributes to OMA-1 degradation in at least 2 ways. First, as noted earlier, CDK-1 activates MBK-2 during the progression though meiosis. Second, since no general defects associated with failure to activate MBK-2 are observed in cdk-1 (ne236 and ne2257) alleles, CDK-1 independently promotes OMA-1 degradation downstream of MBK-2 activation during the first mitosis. However, interestingly, CDK-1 does not directly phosphorylate OMA-1, and target(s) of CDK-1 required for OMA-1 degradation remains mysterious. Despite the fact that the molecular link tying CDK-1 activity to OMA-1 destruction is still missing, it is clear that CDK-1 is embedded in the web of regulatory mechanisms that orchestrate the transition from oogenesis to embryogenesis, for example by providing the timing cue that couples OMA-1 destruction to the first mitosis.

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Figure 3. (A) Model for the role of CDK-1 in OMA-1 degradation during oocyte-to-embryo transition. CDK-1 functions together with conserved protein kinases, for example, MBK-2, to promote the timely destruction of zinc-finger protein OMA-1 during the first mitosis. Removal of OMA-1 allows the protein degradation machinery to downregulate the levels of various cell fate determinants for asymmetric inheritance and release of sequestered TAF-4, a component crucial for the assembly of the transcription factor-II D (TFIID) and the RNA polymerase II complex in zygotic gene expression. CDK-1 also functions during the progression through meiosis to phosphorylate and activate MBK-2, which is sequestered on the cortex by EGG-3/4/5, until anaphase-promoting complex degrades EGG-4/5 and releases MBK-2 to cytoplasm. Upon release from the cortex, MBK-2 phosphorylates OMA-1 and starts the sequential phosphorylation events; however, the destruction of OMA-1 is delayed until the first mitosis when CDK-1 is again activated. (B) Model for CDK-1 function in regulating asymmetric cell division of EMS cell. CDK-1 phosphorylation of WRM-1 together with modifications induced by Wnt signaling releases WRM-1, an inhibitor of spindle rotation, from the posterior cortex of EMS, thereby exposing a polarity cue (red solid line) that captures one of the astral microtubules (brown arrow) and rotates the mitotic spindle in alignment with the anterior–posterior axis of embryo. Wnt signal and Src signal reinforce the capturing and/or pulling of astral microtubule. Modified WRM-1 (for example by phosphorylation) released from the posterior cortex of EMS accumulates preferentially in the posterior nascent nucleus and drives the endodermal fate.

The Role of Cyclin E in Regulating the Transition from Germ Cell Proliferation to Meiotic Differentiation in C. elegans

The C. elegans germline consists of 2 U-shaped gonad arms, one anterior and one posterior, that are connected at the uterus.³⁹ In each gonad arm, the distal end (relative to the uterus) harbors a stem cell niche of proliferating germ cells known as the “mitotic zone” (Fig. 4A). However, unlike other stem cell systems, in which a small number of stem cells divide asymmetrically, the C. elegans mitotic zone harbors more than 200 syncytial cells that divide into equivalent daughters. The fate of these daughters is not determined by asymmetric division, but rather by their position relative to the niche signal. The proliferative mode of the mitotic zone is promoted by Notch signaling from the somatic–gonadal distal tip cell (DTC).^40,41 The DTC expresses the transmembrane LAG-2/Delta ligand, which activates the GLP-1/Notch receptor in germ cells, triggering cleavage and nuclear translocation of the Notch intracellular domain (ICD). The GLP-1 ICD interacts with CSL family transcription factors to regulate the expression of genes necessary for the proliferation of germ cells (Fig. 4B).⁴² Thus, under the influence of the DTC, germ cells are maintained in mitosis. However cell division within the distal region gradually causes germ cell nuclei to move away from the DTC and to enter the transition zone, where they exit mitosis and initiate meiosis. GLD-1 is a KH domain RNA binding protein that accumulates at low levels in the distal end of the germline but gradually rises until reaching maximum levels in the transition zone. In the absence of GLP-1/Notch signaling, GLD-1 is ectopically expressed in the distal region of the germline.⁴³ Conversely, overexpression of GLD-1 in the distal end abrogates the proliferative fate and causes germ cells to enter meiosis prematurely. Consistent with these observations, GLD-1 binds the 3′UTR of glp-1 mRNA and represses its translation in the embryo and meiotic region of the germline.⁴⁴ Collectively, these genetic and biochemical interactions suggest a mutual repressive feedback between Notch-backed proliferation and GLD-1-based differentiation (Fig. 4B).

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Figure 4. (A) Transition from mitosis into meiosis in C.elegans germline. The Distal Tip Cell (DTC in green) caps the distal end of the germline and induces mitotic proliferation (blue). Beyond the reach of the DTC Notch signaling, germ cells transition into the differentiation zone in a GLD-1 dependent manner, where they undergo meiosis (red). (B) Model for Cyclin E in maintenance of germ stem-cell fate in C. elegans. The boundary between the proliferative and transition zones is maintained by 2 mutual negative regulations: CDK-2/ CYE-1 and GLP-1 inhibit accumulation of GLD-1 in the mitotic proliferation zone, while GLD-1 represses the translation of cye-1 and glp-1 transcripts in the transition zone. It remains to be seen if CYE-1 can maintain proliferation zone by enhancing GLP-1 ICD induction in the similar way it does in vulval development.

The proliferative fate has also been shown to depend on CDK-2/CYE-1(Cyclin E), since premature meiotic differentiation is enhanced in a weak glp-1 mutant background upon cye-1 or cdk-2 RNAi.⁴⁵ CDK-2/CYE-1 directly phosphorylates GLD-1 in vitro, and cye-1 RNAi leads to an increase in GLD-1 levels in the distal end of the gonad. Since mutating the phosphorylation site in GLD-1 phenocopies this increase in distal GLD-1 levels, it is likely that that CDK-2/CYE-1 functions in the distal region of the gonad to block the premature switch to meiotic differentiation by targeting GLD-1 directly (Fig. 4B).⁴⁶ Interestingly, GLD-1 binds to the 3′UTR of cye-1 and represses its translation, emphasizing the mutual negative feedbacks that govern proliferation vs. differentiation decisions in the germline (Fig. 4B).⁴⁸ However interestingly, reduction of cdk-2 or cye-1 function leads to premature meiotic entry even in the absence of gld-1. Therefore CDK-2/CYE-1 must also promote proliferation through a GLD-1 independent pathway.

The role of Cyclin E in C. elegans vulval development may offer a clue to this additional mode of action. During vulva development in C. elegans, the anchor cell (AC) signals the induction of a primary vulval precursor cell (VPC) P6.p, via the EGFR signaling pathway. Upon induction, P6.p then signals its neighboring VPCs P5.p and P7.p, via the LIN-12/Notch signaling pathway, to adopt secondary fates. By utilizing a NICD::GFP reporter, it was demonstrated that CYE-1 exerts a stabilizing effect on the intercellular pool of NICD in VPCs.⁴⁷ It is enticing to surmise that CYE-1 may exert a similar stabilizing effect on GLP-1 ICD in the germline mitotic zone. If this indeed is the case, then Cyclin E would maintain the proliferative mode of mitotic germ cells by both positively stabilizing the GLP-1/Notch proliferative cue and negatively targeting GLD-1 to prevent the transition to meiosis (Fig. 4B).

Conclusion

In addition to executing DNA synthesis and mitosis, dividing cells must compute crucial developmental decisions such as division orientation and identity. Because of their central role in regulating cell division, CDK cyclin complexes are ideal factors for mediating the multifaceted decisions required to ensure the overall coherence of developmental programs. The examples reviewed here identify common themes that cells use to couple cell division and differentiation. External cues provide spatial orientation to dividing cells within a larger developmental context (e.g., P2, DTC, and AC). Internal cellular components, such as centrosomes and microtubules, provide early reference points for future daughter cells. Cyclins provide temporal orientation, defining the phase through which a dividing cell is passing. CDKs provide a molecular switch, modifying targets to regulate their activity or stability. Using these tools, cells are able to segregate cell fate determinants to specific daughter cells, activate proteins at a certain stage of division and within a certain spatial context, or destroy them after fulfilling their role. The coordination of these events ensures the accurate progression of development. It seems likely that the molecular connections between the cell cycle machinery and developmental regulation will become more prominent in the future, as additional CDK substrates important for specific developmental processes are identified. For example, Xenopus CDK14 (a CDK1 variant) bound to membrane-tethered Cyclin Y promotes Wnt signal transduction by phosphorylating the low-density lipoprotein receptor-related protein 5 and 6 (LRP5/6) co-receptor during the G₂/M phase of the cell cycle.⁴⁹ The identification of CDK1 substrates important for developmental regulation will improve our understanding of the role of CDK1/cyclin in regulating development.

A recurrent challenge facing the analysis of a major cell cycle regulator such as CDK1 in development has been its obligatory role in cell cycle progression. The studies summarized in this review provided unique opportunities to identify additional roles of CDK1 by genetically uncoupling developmental decisions from cell cycle regulation. These studies also underscore the value of forward genetics in model organisms to identify rare and useful alleles of essential genes, for which the strong loss-of-function (e.g., null alleles or RNAi) cause pleiotropy that masks more subtle functions. Given the conservation and fundamental importance of CDKs and cyclins, their roles in regulating differentiation as identified in flies and worms are very likely to be conserved in mammals.

Disclosure of Potential Conflicts of Interest

Acknowledgments

References