Mechanism of G1 arrest in the Drosophila eye imaginal disc

BioMed Central Page 1 of 13 (page number not for citation purposes) BMC Developmental Biology Open Access Research article Mechanism of G1 arrest in the Drosophila eye imaginal disc Luis M Escudero and Matthew Freeman* Address: MRC Laboratory of Molecular Biology, Hills Road, Cambridge CB2 0QH, UK Email: Luis M Escudero - [email protected]; Matthew Freeman* - [email protected] * Corresponding author Abstract Background: Most differentiating cells are arrested in G1-phase of the cell cycle and this proliferative quiescence appears important to allow differentiation programmes to be executed. An example occurs in the Drosophila eye imaginal disc, where all cells are synchronized and arrested in G1 phase prior to making a fate choice either to initiate the first round of photoreceptor differentiation or to re-enter one terminal mitosis. Results: We have analysed the mechanism of this temporally regulated G1-phase in order to develop an integrated model of this proliferative regulation. We find that an overlapping set of cell cycle inhibitors combine to form an efficient barrier to cell cycle progression. This barrier depends on both the primary secreted signals that drive retinal development, Dpp and Hh. Each of these has distinct, as well as partially overlapping functions, in ensuring that Cyclin E and dE2F1 are kept in check. Additionally, inhibition of Cyclin A by Roughex is essential, and this regulation is independent of Dpp and Hh. Conclusion: One implication of these results is to further support the idea that Cyclin A has important functions in S-phase entry as well as in mitosis. The unexpectedly complex network of regulation may reflect the importance of cells being uniformly ready to respond to the inductive signals that coordinate retinal differentiation. Background All eukaryotes use the same fundamental machinery to drive cell cycle progression but multicellular organisms face the additional challenge of regulating the time and place of proliferation throughout development. A well conserved aspect of this developmental regulation is that cells normally arrest in G1-phase of the cell cycle prior to differentiation. This provides a quiescent stage for differentiation to begin and, once cells start to adopt their terminal fate, most will never re-enter a proliferative state. In tumorigenesis, however, re-entry of arrested cells into abnormal proliferation can occur [1]. The Drosophila eye provides an experimentally amenable example of developmentally regulated proliferation and has therefore been extensively studied as a model. Differentiation of the individual facets (ommatidia) of the compound eye occurs in a moving wave from the posterior to the anterior of the eye imaginal disc, implying that there is a gradient of increasing cell maturity from anterior to posterior in the disc. The front of the wave of development is marked by an indentation known as the morphogenetic furrow (MF) [2]. Several hours prior to the passage of the MF (and therefore anterior to it) all cells in the eye disc arrest in G1-phase [3,4]. After the MF passes, those cells that have not yet started to differentiate as photorePublished: 2 March 2007 BMC Developmental Biology 2007, 7:13 doi:10.1186/1471-213X-7-13 Received: 13 September 2006 Accepted: 2 March 2007 This article is available from: http://www.biomedcentral.com/1471-213X/7/13 © 2007 Escudero and Freeman; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. BMC Developmental Biology 2007, 7:13 http://www.biomedcentral.com/1471-213X/7/13 Page 2 of 13 (page number not for citation purposes) ceptors re-enter S-phase for one terminal round of division, the "second mitotic wave" [5]. Here we focus on the mechanisms responsible for establishing and maintaining G1-arrest of cells prior to the MF (in what we call non-proliferative region, NPR). Specifically, we aim to understand how cells become synchronous and arrest in G1-phase and to learn how the signals that drive the wave of eye development direct this process. This aspect of developmental control of proliferation in Drosophila is not well understood, although it has been investigated in a number of different contexts including the eye, the wing and the embryo [4,6-12]. Most significantly in the eye, Decapentaplegic (Dpp, the Drosophila homologue of BMP ligands) signalling is required to maintain G1 arrest in the anterior region of the arrested zone. Dpp appears to repress Cyclin E, since the removal of several CycE inhibitors [7,13,14] causes a similar phenotype to the lack to the Dpp receptor, thick veins (tkv) or to the overexpression of a CycE transgene [12]. More recently, Firth and Baker have concluded that Dpp and Hedgehog (Hh) act redundantly, and between them are sufficient to arrest cells in G1 [7]. This involvement of Dpp and Hh is consistent with their roles as the primary secreted signals that drive MF progression. Finally, the overexpression of Cyclin A or the absence of the cyclin kinase inhibitor Roughex (Rux) can also induce S-phase entry in the NPR [4,15]. Together, these earlier studies have identified a number of different mechanisms of control of G1 arrest but it is notable that no common checkpoint has been identified and no unified view of the process has yet been proposed. Providing an explanation for this lack of a clear model, our results indicate that in the eye disc no single component is fully responsible for the developmental cell cycle arrest prior to the morphogenetic furrow. We show that first, Hh and Dpp together promote entry into mitosis of the cells prior to G1 arrest, thereby driving cells into G1phase and initiating the NPR. Then, an overlapping set of cell cycle inhibitors combine to form an efficient and robust barrier to cell cycle progression. This barrier depends partially on the inhibition of Cyclin E and dE2F1 activity, also under the control of Dpp and Hh. However, in contrast to previous work [7], our results show that the role of Hh and Dpp in maintaining G1 arrest, is largely confined to the anterior part of the NPR. The inhibition of Cyclin A by Rux becomes the major barrier to S-phase entry in the posterior region and, significantly, this is independent of both Dpp and Hh. This analysis of the relative importance of the different players involved in G1 arrest allows us to integrate them into an overall model of signal-regulated synchronisation and proliferative arrest. Results Defining the region of G1 arrest in the eye imaginal disc Between the proliferating cells in the anterior of the eye imaginal disc and the SMW is a broad band of cells that are arrested in G1-phase [3,16]; they span about 11–14 rows of cells. Given the accepted view that the morphogenetic furrow moves forward, on average, by one row of ommatidia (3–4 cell rows) every 70 min [17], we estimate that on average cells remain in this G1 arrest for five to six hours. Interestingly, this is only slightly longer than the estimate of the normal G1 phase of cells in the proliferating region of the disc. This is based on the observation that the doubling time for cells in the eye disc is approximately 12 hours [18], and that the proportion of cells in G1 phase in proliferating disc cells is one third [19]. These estimates imply that the formation of this non-proliferative region (NPR) depends significantly on cell cycle synchronization as they approach the MF, as well as on specific arrest mechanisms. In this paper we define the NPR as corresponding to the absence of BrdU incorporation anterior to the SMW (Fig. 1A–C). So, from anterior to posterior in the eye disc are 1) the region where undifferentiated cells proliferate randomly; 2) the NPR (which includes the morphogenetic furrow); and 3) the second mitotic wave (Fig. 1C). Note that in the anterior part of the NPR, cells do not enter G1 arrest until after mitosis, so the last cells to be detected by BrdU staining actually enter G1 one or two rows later, after completion of G2 and M-phases. The activity of dE2F1 (a homologue of mammalian E2F, a transcription factor responsible for the expression of many S-phase components [20]) is largely absent from the NPR, as measured by the expression of a PCNA-GFP reporter [21], which contains the dE2F1 binding sequence from the promoter of the PCNA gene (Figure 1B, E). We observed that the downregulation of BrdU staining coincides precisely with the onset of Atonal (Ato) expression [22,23] anterior to the furrow (Fig. 1A, B, D), and with the loss of Homothorax (Hth) expression (not shown). However, in clones of ato or hth mutant cells enter G1 arrest normally, implying that these genes are not essential for establishing the NPR. To characterise the anatomy of the NPR further, we have used 3-dimensional reconstruction software to image the disc (Fig. 1D, E). This clearly showed that the morphogenetic furrow forms the posterior region of the NPR. It also allowed a clear view of the 'peripodial membrane', the layer of squamous cells that overlie the disc-proper and which can influence aspects of disc development [24]. BrdU positive cells are present in the peripodial membrane, but these were randomly distributed, indicating the absence of coordination of G1 arrest between the two adjacent epithelia. To prevent the BrdU positive cells in BMC Developmental Biology 2007, 7:13 http://www.biomedcentral.com/1471-213X/7/13 Page 3 of 13 (page number not for citation purposes) the peripodial membrane being misinterpreted as disc proper cells, in all subsequent confocal projections we used Ato expression as a reference for disc proper. The NPR requires repression of Cyclin E, dE2F1 and Cyclin A In Drosophila, the main activators of S-phase entry are Cyclin E [25], dE2F1 [20,26] and Cyclin A [7,9,15,27]. All are inactive in the NPR and the protein levels of Cyclins E and A are very low in this region [4,12]. To examine the relative importance of the absence of these S-phase triggers in the maintenance of G1 arrest, we overexpressed them using the flip-out Gal4 technique [28]. This technique permits the direct comparison between overexpressing cells and neighbouring wild-type cells, thereby providing a more detailed view of the phenotype than is possible with simple Gal4 misexpression. The ectopic expression of Cyclin E induced BrdU incorporation very efficiently in the anterior region of the NPR (Fig. 2A and [12]). More rarely, we observed a few cells in S-phase in more postePattern of proliferation and G1 arrest in the eyeFigure 1 Pattern of proliferation and G1 arrest in the eye. (A) Projection of several confocal sections of a WT eye disc showing Armadillo (green), Elav (red) and Ato (blue) localization. The morphogenetic furrow (MF, arrowhead in all figures) is highlighted by accumulation of Armadillo (β-catenin), which outlines cell membranes. Ato expression appears between 6–8 cells anterior to the MF and becomes limited to the R8 photoreceptor just posterior to the furrow. Elav is expressed in all the photoreceptor cells posterior to the Ato expressing R8. In this and all subsequent figures, anterior is to the left. (B) WT eye disc showing the incorporation of BrdU (red) and the expression of PCNA-GFP reporter (indicating dE2F1 activation, green) and Ato protein (blue). Anterior to the furrow there is a non-proliferative region, without BrdU incorporation (white bar). The pattern of PCNA-GFP expression coincides with the regions of proliferation. (C) Scheme showing the different proliferating regions of the eye disc. The panel shows a drawing of the disc in 1B. The inset shows a picture of the whole disc. From anterior to posterior: orange marks the region of undifferentiated cells that proliferate randomly; the NPR is marked in blue (its extent is marked by the white bar), with the darker zone showing the morphogenetic furrow (also marked by an arrowhead); finally, the red band marks the region of the second mitotic wave. (D) Z-axis reconstruction of a WT eye disc. The outlines of the cells are shown by Armadillo (Arm) expression (green). The peripodial membrane appears at the top with some BrdU positive cells (red). In the disc proper there is a high accumulation of Arm protein in the apical part of the MF (arrowhead). S-phase nuclei in the SMW are basally located (arrow), whereas anterior to the NPR, BrdU positive nuclei are more apical. The NPR includes the furrow cells (that accumulate high apical levels of Arm) and between 4–6 rows of more anterior cells. Ato expressing cells (blue) are restricted to the disc proper. (E) The cytoplasmic expression of PCNA-GFP reporter (blue) is seen in cells that are completing the cell cycle in the most anterior part of the NPR, but is not expressed in the cells of the MF (that accumulate Ecadherin in the apical region, in green). In the SMW the cells with BrdU positive nuclei also express the PCNA-GFP. Elav Ato Arm BrdU Ato PCNA BrdU E-cadh PCNA BrdU Arm Ato AB DE NPR SECOND MITOTIC WAVE AP C BMC Developmental Biology 2007, 7:13 http://www.biomedcentral.com/1471-213X/7/13 Page 4 of 13 (page number not for citation purposes) rior regions of the NPR. Cyclin E regulates dE2F1 activity by inhibiting Rbf [29], the Drosophila homologue of the retinoblastoma factor. Consistent with this, cells overexpressing Cyclin E expressed the dE2F1 reporter construct, PCNA-GFP (Fig. 2B). Overexpression of UAS-dE2F1 (combined with its obligate partner UAS-Dp) [30] caused a weaker phenotype than Cyclin E, although the pattern was similar: in this case, occasional BrdU positive cells were seen but only in the anterior region of the NPR (Fig. 2C). This result is consistent with the loss of function phenotype of rbf, the main inhibitor dE2F1 activity, which causes ectopic Sphase cells only in the most anterior regions of the NPR [13]. Taken together, the overexpression of Cyclin E and dE2F1/Dp in the NPR implies that at least one additional mechanism must promote G1 arrest in the posterior cells of the NPR; unlike the anterior cells, they are refractory to overexpression of Cyclin E or dE2F1/Dp. Note that because of the progressive development of the retina, the anterior cells mature into the posterior cells, so this different responsiveness to Cyclin E and dE2F1/Dp actually represents a developmental difference rather than a spatial one. The co-overexpression of UAS-cycE and UAS-dE2F1/Dp produced a slightly stronger phenotype than UAS-cycE overexpression alone (in which endogenous dE2F1 is also activated): S-phase is efficiently activated in the anterior but less so in the posterior part of the NPR (Fig. 2D). This result is consistent with the earlier report that in clones mutant for both rbf and dap, inhibitors of dE2F1 and Cyclin E, respectively, the cells in the whole of the NPR do not arrest [7]; in our hands these double mutant rbf dap clones can only sometimes induce ectopic BrdU staining in the anterior region of the NPR and have even weaker effects in the posterior region (not shown). We take the difference between the more powerful effect of ectopic Cyclin E and dE2F1, and the weaker effect of rbf dap to indicate that overexpression of activators is a more powerful trigger than removal of natural repressors. Cyclin A has a less well defined role in S-phase activation but the evidence for its participation is nevertheless strong [7,15,27]. Interestingly, its overexpression in the NPR gave a different result to Cyclin E or dE2F1. UAS-cycA induced ectopic BrdU staining in the whole width of the NPR, but was most efficient in the most posterior domain, where Cyclin E and dE2F1 are less effective (Fig. 2E and [15]). The combination of both transgenes, UAS-cycA and UAS-cycE strongly induced ectopic S-phase entry in cells throughout the NPR: almost all overexpressing cells failed to arrest in G1 (Fig. 2F). Overall, our data provide strong evidence that G1 arrest in the NPR is controlled by multiple mechanisms with distinct regional effects. Specifically, in the anterior region of the NPR, which corresponds to the early stages of G1 arrest, the repression of Cyclin E and dE2F1 activity is critically important, while in the posterior half, where the cells are more mature, the repression of Cyclin A becomes necessary for the maintenance of these cells in the G1 phase. Control of G1 arrest by Hh and Dpp The NPR is the earliest visible change in cells as they enter the wave of development that will eventually produce the adult retina. Ultimately, the whole wave of eye development is propagated by secreted Dpp and Hh signals. Consistent with this, it has previously been reported that Dpp is responsible for the G1-arrest in the anterior part of the NPR [8,11]; most recently, Firth and Baker have reported that Dpp and Hh act redundantly to induce the whole NPR [7]. To understand the mechanism in detail by which Dpp and Hh cause cells to exit from proliferation and arrest/synchronise in G1, we genetically blocked the two pathways, either alone or together. We used mutations in Thick Veins (Tkv), the Dpp receptor; Smoothened (Smo), the membrane associated transducer of Hh signalling; Mad, an essential intracellular transducer of Dpp signalling; and Ci, a nuclear effector of Hh signalling. Note that Ci has constitutive repressor activity as well as being a Hhdependent activator [31], implying that loss of Ci is not always equivalent to loss of Smo. For this reason, simultaneous loss of Smo and Tkv represents the best way of analysing the loss-of-function phenotypes of the Hh and Dpp pathways in the eye disc [32,33]. Initial synchronisation of cells as they enter the NPR One of the earliest signs of the NPR is an increase in the number of mitotic cells immediately prior to the G1 arrest region. This is seen in wild type discs as a well defined line of phosphohistone H3 (pH3) positive cells immediately anterior to the NPR (Fig. 3A), and contrasts with the much more sparsely scattered pH3-positive cells further anterior. We observed that in the smo tkv double mutant clones (but not in the tkv or smo clones alone, not shown) this clear alignment of mitotic cells was lost (Fig. 3B), implying that cells were no longer being efficiently driven into mitosis. Note that pH3 only stains cells in for a short period of the cell cycle, so its absence cannot be taken as a sign of proliferative arrest. Instead we interpret this result to indicate a function for Hh and Dpp in accelerating through mitosis those cells that are already 'premitotic' or in later stages of the cell cycle. BMC Developmental Biology 2007, 7:13 http://www.biomedcentral.com/1471-213X/7/13 Page 5 of 13 (page number not for citation purposes) A differential requirement for Dpp and Hh signalling in the posterior and anterior of the NPR Loss of smo alone causes a slight delay in entry to the NPR, by one or two rows of cells, but no ectopic BrdU staining occurs in the rest of the region [7]. We examined clones of tkv as well as double mutant clones for Mad ci, or tkv ci, or smo tkv (Fig. 3C–H). All four mutant conditions caused ectopic BrdU incorporation and Cyclin B expression in the anterior region of the NPR but none caused significant ectopic S-phase induction in the posterior region (this is especially clear in the case of Cyclin B staining (Fig. 3F, 3H). Of these four conditions, smo tkv was the only one in which occasional BrdU positive cells were detected in the posterior region (6 out of 32 clones; no more than 2–3 positive cells in any clone). Three points emerge from these data. First, they imply a clear difference between the maintenance of G1 in the anterior and posterior of the NPR. Second, Firth and Baker reported ectopic BrdU incorporation and Cyclin B accumulation in Mad ci clones in the whole NPR, not just the anterior region. We used the same alleles as they did but did not observe any posterior BrdU staining. Third, there is no evidence for a Effect of overexpression of cyclins in the NPRFigure 2 Effect of overexpression of cyclins in the NPR. All panels except B show BrdU staining (red) of eye disc harbouring different overexpression clones marked with GFP (green). (A) The overexpression of CycE is able to induce ectopic BrdU incorporation with a high efficiency in the anterior part of the NPR, but less so the posterior, where only a few cells enter S phase. (B) The PCNA-GFP reporter (green) is active (arrows) in the CycE overexpression clones (marked by presence of β-gal in red) within the NPR. (C) In dE2F1 overexpression clones there is BrdU incorporation only in the anterior part of the NPR. (D) The overexpression of CycE and dE2F1 can induce incorporation of BrdU in anterior and posterior cells of the NPR. (E) CycA overexpressing cells incorporate BrdU in any part of the NPR, but with a higher efficiency in the posterior part, where most cells are BrdU positive. (F) Simultaneous overexpression of CycE and CycA induces a high proportion of BrdU incorporation in any part of the NPR. U-cycE U-dE2F U-cycE U-cycE U-cycE U-cycA U-cycA U-dE2F1 A A’ B B’ C C’ D D’ E E’ F F’ BMC Developmental Biology 2007, 7:13 http://www.biomedcentral.com/1471-213X/7/13 Page 6 of 13 (page number not for citation purposes) Dpp and Hh control G1 arrest primarily in the anterior of the NPRFigure 3 Dpp and Hh control G1 arrest primarily in the anterior of the NPR. (A) WT eye disc showing the cells in mitosis as marked by phosphohistone H3 antibody (PH3, in red) and the Ato pattern of expression (blue). The white arrow marks the line of synchronized mitosis anterior to the NPR in A and B. In the region anterior to this line the frequency of phosphohistone H3 positive cells is very low (asterisk) (B) Eye disc with a large smo3 tkva12 M+ clone (absence of green). The yellow arrow marks the region where the distinct line of mitosis (pH3, red; the so-called first mitotic wave) is lost. (C) tkva12 clones (absence of green) showing some BrdU positive cells (red) in the anterior part but not in the posterior (arrows). (D) Similarly, in tkva12 ci94 clones (marked by the absence of Ci antibody in green) there are no BrdU positive cells in the posterior region of the NPR (red). The arrows mark some BrdU cells in the anterior part of the NPR. (E-F) Mad12 ci94 clones (marked by absence of Ci, green) stained for BrdU (E) and CycB (F) in red. The arrows mark clones in the posterior part of the NPR where there is no ectopic BrdU incorporation or CycB accumulation. (G) smo3 tkva12 clones (arrows) marked by absence of β-gal, in green (arrows). The picture shows a representative clone in the lower part of the panel with no ectopic BrdU positive cells (red) (H) Ectopic CycB (red) accumulates only in the anterior region of the NPR in smo3 tkva12 clones (absence of green). This is highlighted in clones that span the whole NPR, where there is clear CycB accumulation that does not reach the most posterior cells (arrows). Ci BrdU BrdU Ci CycB CycB BrdU GFP GFP CycB BrdU CycB Ci BrdU BrdU tkv - ci - tkv - Mad - ci - Mad - ci - smo - tkv - smo - tkv - smo - tkv - BrdU PH3 Ato PH3 PH3 BGal PH3 WT A A’ B B’ C C’ D D’ E E’ F F’ G G’ H H’ * BMC Developmental Biology 2007, 7:13 http://www.biomedcentral.com/1471-213X/7/13 Page 7 of 13 (page number not for citation purposes) requirement for Ci in this process: tkv ci clones are indistinguishable from clones of tkv alone. Redundancy of Smo and Tkv in the regulation of dE2F1 activity Loss of tkv and smo together caused ectopic dE2F1 activity (as assayed by PCNA-GFP expression) in the whole NPR (Fig. 4B), while loss of tkv alone activated dE2F1 in the anterior region alone (Fig. 4A); loss of smo alone had no effect on dE2F1 activity (not shown). Therefore both signals contribute, in a partially redundant manner, to the normal downregulation of dE2F1 activity in the NPR. Note that this activation of dE2F1 is not sufficient to induce ectopic S-phase entry in the posterior region of the NPR (recall that there was almost no ectopic BrdU or Cyclin B accumulation in posterior smo tkv clones), which is consistent with our observation above that ectopic dE2F1 is also not sufficient to trigger S-phase in this same region. A non-redundant requirement for Hh signalling in the expression of Dacapo Loss of smo alone abolished the expression of Dacapo (Dap), an inhibitor of CycE activity [34,35]. Careful examination showed that Dap expression begins in the posterior domain of the NPR and remains detectable through to the posterior of the SMW (Fig. 4C, 4D). We observed that Dap expression disappears in the smo3 clones, but not in the tkva12 clones or ci94 clones (Fig. 4C, 4D and not shown). This implies that Dap expression is not dependent on Dpp signalling. The result with ci clones implies that, consistent with earlier reports [36,37], there is no positive role for Ci in Hh signalling in this context. We also observed Dap down regulation when the constitutive Ci repressor form, UAS-ciCELL was overexpressed in clones (not shown). We therefore infer that Hh signalling is needed to remove the Ci repressor form in the NPR, rather than directly activating Dap expression. These genetic experiments with the Hh and Dpp pathways point to several substantial conclusions. 1) Both pathways are required to promote the last coordinated mitosis previous to the G1 arrest. 2) G1 arrest in the anterior region of the NPR depends primarily on Dpp signalling. 3) More generally, G1 arrest is regulated differentially in the anterior and posterior of the NPR; in neither region is Cidependent activation required. 4) There is a redundancy between Hh and Dpp in the control of dE2F1 activity in the posterior of the NPR. 5) There is a non-redundant requirement for Hh to activate Dap expression (and thereby inhibit Cyclin E) in the posterior of the NPR; this activation requires Smo but, again, not Ci. Together, these data imply that while there is some redundancy between Hh and Dpp signalling in the control of the NPR, nonoverlapping functions can also be identified. They also imply that, contrary to an earlier report [7], Hh and Dpp signalling do not comprise the whole mechanism of G1 arrest: in the posterior region of the NPR, some other factor must prevent cells from S-phase entry, even when Hh and Dpp signalling are completely blocked. A secondary role for Atonal in maintaining G1 arrest? Ato expression in the NPR is induced by both Hh and Dpp pathways [32]. Together with the involvement of other proneural genes in G1 arrest in the wing margin [10], this suggests a possible role of this gene in the establishment of the NPR. However, we did not observe ectopic BrdU positive cells in Ato loss-of-function clones encompassing the NPR (Fig. 4E). On the other hand, about 55% of Atonal overexpression clones showed a clear precocious entry into the NPR (Fig. 4F), suggesting that Atonal may influence mitotic progression prior in the NPR. Rux is necessary for the G1 arrest in the NPR The observation that Cyclin A overexpression induced BrdU incorporation in the NPR suggested that Cyclin A inhibition is important for the arrest of these cells. We therefore examined the phenotype of removing Roughex (Rux), a cytoplasmic inhibitor of Cyclin A activity [4,15,38,39]. rux mutant eye discs have increased proliferation anterior and posterior to the morphogenetic furrow [4]. To dissect this phenotype precisely, we induced loss of function clones of the null allele rux8. In distinction to the loss of smo and tkv, cells in the most posterior part of the NPR are no longer arrested in G1, demonstrated by the high number of cells that incorporate BrdU and the accumulation of Cyclin B (Fig. 5A–B); anterior cells are affected only slightly and many remain arrested in G1 (Fig. 5A). This phenotype is similar to that obtained by overexpressing Cyclin A and supports the idea that Rux represses Cyclin A activity and plays a significant role in maintaining G1 arrest, particularly in the posterior of the NPR. rux8 clones also displayed slight ectopic activation of the PCNA-GFP transgene in the NPR (Fig. 5C) suggesting that the powerful activation of S-phase in these clones might rely on more than just Cyclin A activation. However, since Rux is reported to be a specific regulator of Cyclin A, and is therefore not expected to affect dE2F1 activity directly, we tested whether this upregulation of dE2F1 was triggered by Cyclin A activity. Indeed, Cyclin A overexpression was also able to induce weakly the PCNA reporter in the NPR (Fig. 5D), suggesting that the slight gain of dE2F1 activity in rux clones was indirect. Rux antibodies are not sensitive enough to detect the endogenous protein by immunofluorescence, so the expression pattern of rux in the eye disc was analysed using a rux-lacZ transgene that is able to rescue the rux phenotype and is therefore thought to represent faithfully the expression of the gene [15]. rux-lacZ is expressed gen- BMC Developmental Biology 2007, 7:13 http://www.biomedcentral.com/1471-213X/7/13 Page 8 of 13 (page number not for citation purposes) erally in the eye disc, including in the NPR, with a decrease just posterior to the morphogenetic furrow as the second mitotic wave initiates (Fig. 5F). Expression of rux was not dependent on Dpp or Hh signalling: rux-lacZ was not down-regulated in smo tkv double mutant clones. On the contrary, rux-lacZ was elevated, indicating that Hh and Dpp normally repress rux expression in the second mitotic wave (Fig. 5G). This result is consistent with our other data that imply that Hh and Dpp are important determinants of G1 arrest only in the anterior domain of the NPR. In the posterior domain, when the cells have developed further, Cyclin A and Rux become the key regulators of G1 arrest. Discussion Mitotic synchrony vs. G1 Arrest In this paper we have focused on the mechanism of G1 arrest in the eye imaginal disc, the first overt sign of retinal differentiation. Although the NPR has sometimes been considered to be merely the beginning of the morphogenetic furrow, our 3D image analysis clearly shows that it initiates well before the cells alter their shape. Just anterior to the cells arrested in G1, there is a increased number of mitotic cells suggesting a coordinated activation of their entry into mitosis. This could represent the subset of cells that are in S or G2 phases and that are accelerated through the cell cycle in order to become arrested in G1. We have Factors contributing to G1 arrestFigure 4 Factors contributing to G1 arrest. (A-B) PCNA-GFP expression (green) in discs with tkva12 (A) and smo3 tkva12 (B) clones. Upregulation in the posterior part of the NPR only occurs in the smo3 tkva12 clones. (C-D) Eye disc with smo3 (C) and tkva12 (D) clones (absence of GFP in red), stained for Dap antibody in green. The loss of smo, but not tkv, causes the loss of Dap in the furrow (arrows). (E) Eye disc with ato1 M+ clones (absence of green) showing no ectopic BrdU incorporation (red) in the NPR. (F) UAS-ato overexpression clones (marked by GFP in green) can inhibit CycB accumulation (red) close to the anterior part of the NPR (arrow in F'). BMC Developmental Biology 2007, 7:13 http://www.biomedcentral.com/1471-213X/7/13 Page 9 of 13 (page number not for citation purposes) shown that Hh and Dpp both have a novel role in this first mitotic synchronisation. This could be mediated by String (the homologue of Cdc25 phosphatase in Drosophila) since its RNA is upregulated in these cells [4]. Obviously, not all cells will be poised to enter mitosis immediately upon receiving these signals but we imagine that their function is to drive cells through mitosis with as little delay as possible. Based on several lines of published evidence and our data [17-19], we estimate that cells in the NPR spend only a little more time in G1 phase than the proliferating anterior cells of the eye disc (see above). Coupled with the sharp onset of G1-arrest, this implies that the NPR is at least partly a consequence of cells being triggered to enter G1 synchronously. However, the observation that the loss of tkv causes ectopic S-phase entry in the anterior part of the NPR, and the fact that G1-phase is extended, albeit not greatly, both indicate the existence of a mechanism for preventing cells precociously entering S-phase in the NPR. In other words, we conclude that the NPR is a conseRux is necessary to maintain G1 arrest in the posterior of the NPRFigure 5 Rux is necessary to maintain G1 arrest in the posterior of the NPR. (A-B) rux8 clones (absence of β-galactosidase in green) stained for BrdU (A) and CycB (B) in red. Both ectopic BrdU incorporation and CycB accumulation lie predominantly in the posterior part of the NPR, although occasional BrdU positive cells are also seen more anteriorly. (C-D) PCNA-GFP reporter expression (green in C and D, and white in C' and D') in discs with rux8 clones (absence of red in C) and CycA overexpression clones (marked by presence of β-galactosidase (red in D). The PCNA-GFP reporter is slightly activated in the rux clone in the NPR (arrow in C') and in cells overexpressing CycA in the NPR (arrow in D'). (F-G) rux-lacZ transgene expression (red) in a WT disc (F) and in a disc harbouring smo3 tkva12 double mutant clones. The transgene is expressed in the NPR, the position of which is localised by the expression of Ato (blue in F), and its levels decreases just posterior to the MF. The levels of rux-lacZ increase in the double mutant cells for smo and tkv (marked by absence of green in G). The bar indicates the width of the NPR.