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Dual roles for the Dab2 adaptor protein in embryonic development and kidney transport

2002; Springer Nature; Volume: 21; Issue: 7 Linguagem: Inglês

10.1093/emboj/21.7.1555

1460-2075

Shelli M. Morris,

Genetic and Kidney Cyst Diseases

Article1 April 2002free access Dual roles for the Dab2 adaptor protein in embryonic development and kidney transport Shelli M. Morris Shelli M. Morris Fred Hutchinson Cancer Research Center, Division of Basic Sciences, 1100 Fairview Avenue North, Seattle, WA, 98109 USA Search for more papers by this author Michelle D. Tallquist Michelle D. Tallquist Fred Hutchinson Cancer Research Center, Division of Basic Sciences, 1100 Fairview Avenue North, Seattle, WA, 98109 USA Present address: Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, 75390 USA Search for more papers by this author Charles O. Rock Charles O. Rock St Jude Children's Research Hospital, Protein Science Division, Department of Infectious Diseases, Memphis, TN, 38101 USA Search for more papers by this author Jonathan A. Cooper Corresponding Author Jonathan A. Cooper Fred Hutchinson Cancer Research Center, Division of Basic Sciences, 1100 Fairview Avenue North, Seattle, WA, 98109 USA Search for more papers by this author Shelli M. Morris Shelli M. Morris Fred Hutchinson Cancer Research Center, Division of Basic Sciences, 1100 Fairview Avenue North, Seattle, WA, 98109 USA Search for more papers by this author Michelle D. Tallquist Michelle D. Tallquist Fred Hutchinson Cancer Research Center, Division of Basic Sciences, 1100 Fairview Avenue North, Seattle, WA, 98109 USA Present address: Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, 75390 USA Search for more papers by this author Charles O. Rock Charles O. Rock St Jude Children's Research Hospital, Protein Science Division, Department of Infectious Diseases, Memphis, TN, 38101 USA Search for more papers by this author Jonathan A. Cooper Corresponding Author Jonathan A. Cooper Fred Hutchinson Cancer Research Center, Division of Basic Sciences, 1100 Fairview Avenue North, Seattle, WA, 98109 USA Search for more papers by this author Author Information Shelli M. Morris1, Michelle D. Tallquist1,2, Charles O. Rock3 and Jonathan A. Cooper 1 1Fred Hutchinson Cancer Research Center, Division of Basic Sciences, 1100 Fairview Avenue North, Seattle, WA, 98109 USA 2Present address: Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX, 75390 USA 3St Jude Children's Research Hospital, Protein Science Division, Department of Infectious Diseases, Memphis, TN, 38101 USA *Corresponding author. E-mail: [email protected] The EMBO Journal (2002)21:1555-1564https://doi.org/10.1093/emboj/21.7.1555 PDFDownload PDF of article text and main figures. ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinked InMendeleyWechatReddit Figures & Info The Disabled-2 (Dab2) gene has been proposed to act as a tumor suppressor. Cell culture studies have implicated Dab2 in signal transduction by mitogens, TGFβ and endocytosis of lipoprotein receptors. To identify in vivo functions of Dab2, targeted mutations were made in the mouse. In the absence of Dab2, embryos arrest prior to gastrulation with a phenotype reminiscent of those caused by deletion of some TGFβ signal transduction molecules involved in Nodal signaling. Dab2 is expressed in the extra-embryonic visceral endoderm but not in the epiblast. Dab2 could be conditionally deleted from the embryo without affecting normal development, showing that Dab2 is required in the visceral endoderm but dispensable in the embryo proper. Conditionally mutant Dab2−/− mice are overtly normal, but have reduced clathrin-coated pits in kidney proximal tubule cells and excrete specific plasma proteins in the urine, consistent with reduced transport by a lipoprotein receptor, megalin/gp330, in the proximal tubule. This evidence indicates that Dab2 is pleiotropic and regulates both visceral endoderm function and lipoprotein receptor trafficking in vivo. Introduction The Disabled-2 (Dab2)/DOC2 gene is widely expressed in at least two alternative splice forms, encoding p96 and p67 proteins (Mok et al., 1994; Xu et al., 1995). Expression of Dab2 is decreased in many ovarian, mammary and prostate carcinomas, and in choriocarcinomas (Fulop et al., 1998; Mok et al., 1998; Schwahn and Medina, 1998; Tseng et al., 1998; Fazili et al., 1999). Dab2 expression inhibits proliferation of cultured cells, suggesting that its down-regulation is important for tumor initiation or progression (Tseng et al., 1998; Sheng et al., 2000). However, the cellular basis for this apparent tumor suppressor effect and the normal functions of Dab2 are unknown. Both Dab2 and a related protein, Dab1, have features of cytoplasmic adaptor proteins, such as protein binding domains, phosphorylation sites and the absence of catalytic domains (Xu et al., 1995; Howell et al., 1997), and may thus participate in signal transduction pathways or regulate protein traffic inside cells (Pawson and Scott, 1997; Pearse et al., 2000). Indeed, Dab1 has an important signaling function during development, regulating migrations of committed but undifferentiated neurons. Genetically, Dab1 relays signals from specific lipoprotein receptors (Rice and Curran, 1999). Lipoprotein receptors are best known for their roles in importing proteins and lipids into cells, but they also have signal transduction functions (Krieger and Herz, 1994; Howell and Herz, 2001). In vitro, both Dab1 and Dab2 bind to a common sequence present in the cytoplasmic tails of lipoprotein receptors, via their phosphotyrosine binding/protein interaction (PTB/PID) domains (Trommsdorff et al., 1998; Howell et al., 1999; Margolis, 1999; Morris and Cooper, 2001). The Dab-binding sequence is also involved in trafficking lipoprotein receptors into the endocytic pathway (Chen et al., 1990). Dab2 has been found in complexes with a lipoprotein receptor, megalin (gp330/gp600), in kidney (Oleinikov et al., 2000), suggesting it could regulate megalin trafficking or signaling. In addition, the p96 splice form of Dab2 binds to the clathrin adaptor AP-2 and localizes to clathrin-coated pits, but it is not known whether p96 regulates endocytosis (Morris and Cooper, 2001). A possible molecular mechanism for growth inhibition by Dab2 is provided by the observation that overexpression of Dab2 can interfere with mitogenic growth factor signal transduction, possibly by inhibiting Ras or MAP kinase activation (Xu et al., 1998; Tseng et al., 1999; Smith et al., 2001; Zhou and Hsieh, 2001). An alternative possible mechanism derives from studies on a TGFβ-non-responsive mutant cell line (Hocevar et al., 2001). These mutant cells express low levels of an altered form of Dab2, and expression of wild-type Dab2 restores TGFβ responsiveness. Moreover, Dab2 associates with TGFβ receptors and with their substrates, the transcription factors SMAD2 and SMAD3 (Hocevar et al., 2001). Since TGFβ inhibits proliferation of some cells, Dab2 may act as a tumor suppressor by promoting TGFβ signaling. TGFβ-related factors relay many inductive signals during mouse embryonic development (Hogan, 1996; Zimmerman and Padgett, 2000). One such factor, Nodal, is important for establishing the anterior–posterior (A-P) axis, induction of mesoderm and definitive endoderm, and left–right asymmetry (Beddington and Robertson, 1999; Schier and Shen, 2000; Lu et al., 2001). The A-P axis is established at the egg cylinder stage, when the embryo proper is represented by a layer of embryonic ectoderm (epiblast) sheathed in a layer of extra-embryonic visceral endoderm (VE). The embryo is attached proximally to maternal tissues via more extra-embryonic cells. Nodal expression is first induced in a proximal-to-distal wave through the epiblast, and then induces the VE at the distal tip to express various genes, change shape and migrate up one side of the epiblast. This altered region of the VE is known as the anterior VE (AVE). Proteins made by the AVE include secreted inhibitors that act back on the epiblast and inhibit Nodal action. Nodal activity is thus restricted to the part of the epiblast most distant from the AVE, which is induced to form mesoderm and defines the future posterior of the embryo. The signal transduction pathways utilized by Nodal in the epiblast cells and VE cells are still being established. However, analysis of mouse mutants reveals that some TGFβ signaling components are needed for signal transduction by Nodal in the epiblast, and others for signal transduction in the VE. We have used a targeted genetics approach to test whether Dab2 regulates signaling or transport in vivo. Our results suggest that Dab2 is needed in the VE, in part to express Nodal-induced genes, and also regulates protein transport in the kidney. Thus Dab2 is pleiotropic, with direct or indirect functions in both signal transduction and protein traffic. Results Targeting of the Dab2 locus The Dab2 gene was subjected to targeted deletion in embryonic stem (ES) cells to simultaneously prepare null and conditional alleles (Figure 1A; Gu et al., 1994). A loxP site for Cre-mediated recombination (Sternberg and Hamilton, 1981) was inserted 5′ to the second coding exon, and a neomycin selection cassette flanked by loxP sites was inserted 3′ to the second exon. Cre recombinase was then transiently expressed from either of two plasmids. Expression from a strong promoter (phosphoglycerate kinase, PGK) allowed recombination between the first and third loxP sites, removing the second coding exon and the neomycin cassette and creating a null allele (Dab2−). The second coding exon encodes the beginning of the PTB domain and is found in all known Dab2 splice forms (Xu et al., 1995; Tseng et al., 1998; Cho et al., 1999; Fazili et al., 1999). If, by chance, splicing should occur from the first to third coding exon, a frameshift would occur, resulting in a truncated protein lacking most of the PTB domain. Expression from a weak promoter (cytomegalovirus, CMV) allowed recombination between the second and third loxP sites, removing the neomycin cassette but leaving the second coding exon flanked by loxP sites (floxed) (Dab2fl allele). Recombined clones were identified by PCR and verified by Southern blotting. ES cells from each type of recombination event were injected into blastocysts, and the resulting chimeric mice were mated in order to generate either Dab2+/− or Dab2fl/+ mice (Figure 1B and C). Figure 1.Targeted disruption of the Dab2 gene. (A) Dab2 targeting strategy. (1) Schematic representation of the Dab2 protein. The parallel lines indicate the region of the Dab2 protein encoded by the second coding exon and targeted for deletion. (2) Partial restriction map of the Dab2 genomic locus in which the initiation ATG is indicated by the arrowhead. (3) Targeting vector containing the diphtheria toxin gene (dt) under the control of the RNA polymerase 2 promoter (P2) and the neomycin resistance gene (neo) under the control of the PGK promoter. LoxP sites are indicated by the triangles. (4) The targeted Dab2 locus prior to Cre expression. (5) The floxed Dab2 allele (Dab2fl) and (6) the deleted Dab2 allele (Dab2−) following Cre expression. Restriction enzymes: H, HpaI; N, NcoI; B, BamHI; S, SmaI; RI, EcoRI; RV, EcoRV. (B) Southern blotting analysis of DNA prepared from a wild-type mouse (lane 1), or mice heterozygous for either the deleted (lane 2) or floxed (lane 3) allele. DNA was digested with NcoI and hybridized to the radiolabeled Dab2 probe shown in (A). The positions of the wild-type (3.0 kb, +), null (2.1 kb, −) and floxed (3.2 kb, fl) alleles are indicated. (C) PCR analysis of P8 pups born from a Dab2fl/+ × Dab2+/− mating. The positions of the wild-type (460 bp, +), null (250 bp, −) and floxed (530 bp, fl) alleles are indicated. The positions of the three PCR primers used (p1, p2 and p3) are indicated by arrows in (A). Download figure Download PowerPoint Dab2 is required for early post-implantation development Dab2 heterozygous mice were fertile and phenotypically normal. To study the phenotype of Dab2 homozygous mice, Dab2+/− mice were intercrossed. Homozygous mutation of Dab2 is lethal in early development, as shown by the absence of Dab2−/− pups and E11.5 embryos, although at E11.5, there were a significant number of sites where dead embryos had been resorbed (Table I). Between E7.5 and E8.5, Dab2−/− embryos were found at the proper Mendelian ratio (Table I; Figure 2A), but they were significantly smaller than their littermates (Figure 2B). These embryos resembled the early egg cylinder stage, indicating that the Dab2 null embryos implant but fail to undergo gastrulation. Figure 2.Analysis of Dab2+/− intercrosses. (A) PCR genotyping of E7.5 embryos resulting from Dab2+/− intercrosses. (B) Morphology of wild-type (+/+) and Dab2 null (−/−) E7.5 and E9 embryos. Download figure Download PowerPoint Table 1. Genotypes of offspring from Dab2+/− × Dab2+/− matings Age +/+ +/− −/− Resorbed P10 110 (37%) 186 (63%) 0 (0%) N/A E11.5 11 (47%) 16 (59%) 0 (0%) 9 E8 8 (24%) 17 (52%) 8 (24%) 0 E6.5 and E7.5 mutant and wild-type embryos were examined by light and electron microscopy (Figure 3). At E6.5, wild-type embryos contain two layers of extra-embryonic (or primitive) endoderm, the outer parietal endoderm (PE) and inner VE, which surround the epiblast (EE) and the developing mesoderm. At the proximal end, trophoblast cells invade the endometrium to form the ectoplacental cone (EPC). Dab2 null embryos contain three layers that resemble the PE, VE and EE of wild- type embryos (Figure 3A and B). However, the Dab2−/− embryos were significantly smaller than their wild-type littermates, and the surrounding yolk sac cavity, between VE and PE, appeared larger. The cells of the presumed EE were jumbled, and not arranged in an epithelial sheet. The proamniotic cavity, inside the embryo, was smaller. By E7.5, the difference in size between wild-type and mutant embryos was even more obvious. At this stage in wild-type embryos, amnion, chorion and allantois had formed in the proximal part of the egg cylinder, mesoderm was invading between EE and VE, the cells of the EE were well organized, and the VE took on a thinner, more squamous morphology (Figure 3C and E). In contrast, the Dab2−/− embryos failed to grow, the amnion, chorion and allantois were absent, and the internal cells of the presumptive EE were disorganized (Figure 3D and F). Additionally, at the distal tip of Dab2−/− embryos, cells of the VE maintained their cuboidal morphology (Figure 3F). Electron microscopy (EM) of thin sections of E7.5 embryos revealed that the mutant VE was composed of well-differentiated epithelial cells with microvilli and apical junctional complexes (Figure 3G and H). This suggests that Dab2 is not needed for epithelial cell differentiation. Figure 3.Histology of wild-type and mutant Dab2 embryos. (A and B) Hematoxylin and eosin-stained sections of E6.5 wild-type (A) and mutant (B) embryos. (C and D) Hematoxylin and eosin-stained sections of E7.5 wild-type (C) and mutant (D) embryos. (E and F) Toluidine blue-stained thin sections from E7.5 wild-type (E) and mutant (F) embryos. (G and H) EM of E7.5 wild-type (G) and mutant (H) visceral endoderm. Bar = 2 μm. (I and J) TUNEL staining (arrows) of E6.5 wild-type (I) and mutant (J) embryos. ve, visceral endoderm; pe, parietal endoderm; ee, embryonic ectoderm; epc, ectoplacental cone; ch, chorion; am, amnion; mes, mesoderm; ysc, yolk sac cavity; jc, junctional complex; mv, microvilli. Download figure Download PowerPoint To determine whether apoptosis is involved in the embryonic lethality, the TUNEL (TdT-mediated dUTP-biotin nick end labeling) assay was performed on E6.5 wild-type and mutant embryos (Figure 3I and J). An overall increase in TUNEL-positive brown nuclei (arrows) was observed in all of the Dab2−/− embryos analyzed as compared with wild-type embryos. This overall increase in apoptosis may contribute to the small size of Dab2−/− embryos. Dab2 is expressed in the visceral endoderm E6.5 embryos were analyzed to identify the sites of Dab2 protein expression (Figure 4). In wild-type embryos, a strong Dab2 positive signal was observed only in the cells of the VE (Figure 4A, asterisk). Staining with the secondary antibody only yielded low non-specific background staining of the PE and maternal tissues (Figure 4B). In the smaller mutant embryo, no Dab2 staining was observed in the VE (Figure 4C). In E7.5 wild-type embryos, Dab2 protein expression was still restricted to the VE (Figure 4D), as reported previously for Dab2 mRNA (Morrisey et al., 2000). Thus, Dab2 protein expression is restricted to the VE at the time when Dab2−/− embryos cease developing normally. Figure 4.Embryonic expression of the Dab2 protein by immunohistochemistry. (A) Dab2 positive staining of the VE in a E6.5 wild-type embryo. (B) Background reaction with secondary antibody only. (C) Immunohistochemistry of a Dab2 null E6.5 embryo. The hatched box indicates the enlarged region. The asterisk indicates the visceral endoderm. (D) Dab2 staining of a E7.5 wild-type embryo. Note that VE is replaced by definitive endoderm at the distal tip at this stage. ve, visceral endoderm; pe, parietal endoderm; ee, embryonic ectoderm; epc, ectoplacental cone; ch, chorion; am, amnion; all, allantois; ysc, yolk sac cavity. Download figure Download PowerPoint Functional defects in Dab2−/− visceral endoderm Coucouvanis and Martin (1995) showed that growth and cavitation of the inner cell mass in vitro depend on signals from the surrounding primitive endoderm. To investigate whether the primitive endoderm of Dab2 mutants can provide such signals, blastocysts were collected at E3.5 from Dab2+/− inter-crosses and cultured for 9 days (Figure 5; Table II). During the first 3–5 days in culture, wild-type, heterozygous and knock-out blastocysts attached to the dish and trophoblastic cells migrated out over the substrate (Figure 5A–C). Between days 5 and 9, the inner cell masses of 83% (25 out of 30) of the wild-type and heterozygous blastocysts expanded and formed large fluid-filled cavities (Figure 5D and E). In most cultures, migrating parietal endoderm cells were visible. In contrast, the inner cell masses of 93% (14 out of 15) of Dab2−/− blastocysts were significantly reduced in size or absent (Figure 5F). Figure 5.In vitro blastocyst outgrowths. (A) Wild-type, (B) heterozygous and (C) mutant blastocysts after 5 days in culture. The same (D) wild-type, (E) heterozygous and (F) mutant blastocysts after 9 days in culture. ICM (arrow), inner cell mass; T (arrowhead), trophectoderm; PE, parietal endoderm. Download figure Download PowerPoint Table 2. Genotype and size of inner cell mass of cultured blastocysts +/+ or +/− −/− Small 5 14 Large 25 1 P > 0.9995. The Dab2−/− phenotype, including failure to thin the distal tip VE, elongate the extra-embryonic portion of the egg cylinder and properly organize the epiblast, resembles those of certain SMAD2 and SMAD4 mutants, in which the distal tip VE fails to differentiate into AVE in response to a Nodal signal (Nomura and Li, 1998; Sirard et al., 1998; Waldrip et al., 1998; Weinstein et al., 1998; Yang et al., 1998). Moreover, when tested, blastocysts or embryoid bodies from SMAD4 mutants failed to grow in vitro (Sirard et al., 1998; Yang et al., 1998). Therefore, we tested for the induction of the AVE markers Cerr1 (Shawlot et al., 1998) and Hex (Thomas et al., 1998). In E6.5 wild-type and heterozygous embryos, Cerr1 and Hex are expressed in the AVE (Figure 6A and C). In contrast, Cerr1 expression and Hex were not detected in Dab2 mutants (Figure 6B and D), suggesting a defect in receipt of the Nodal signal by the distal tip VE. Nodal expression was detected in the embryonic portions of the wild-type and Dab2 mutant egg cylinders (Figure 6E and F), consistent with Dab2-independent expression in the epiblast. Figure 6.In situ hybridization analysis. Cerr1 (A and B), Hex (C and D) and Nodal (E and F) expression in Dab2 wild-type (A, C and E) and mutant (B, D and F) E6.5 embryos. The bracket indicates a signal in the AVE in (A) and (C), and in the distal portion of the embryo in (E) and (F). Download figure Download PowerPoint Rescue of Dab2-deficient embryos with Dab2 in extra-embryonic tissues Because Dab2 expression was only detected in extra-embryonic tissues, we tested whether we could rescue the lethality of Dab2 deletion by selectively removing Dab2 from the embryo proper. Mice homozygous for the conditional Dab2fl allele (Figure 1) were mated to mice heterozygous for the Dab2 null allele and expressing Cre under the control of the Meox2 promoter (Dab2+/−; Meox2cre/+). The expression of the Cre recombinase from Meox2cre is limited to cells of the embryo proper, thus allowing for deletion of floxed alleles only in the embryo (Tallquist and Soriano, 2000). Analysis of E11.5 embryos revealed that mice whose extra-embryonic tissues were Dab2fl/−; Meox2cre/+ were normal in appearance (Figure 7A). Indeed, Dab2 conditionally null animals were born and survived, as shown by PCR genotyping of post-natal day 8 (P8) tail samples (Figure 7B). Immunoblots of P8 tail samples showed that Dab2 protein expression was essentially ablated in the conditionally null mice (Figure 7C). Both p96 and p67 were detected in the tails of mice with one (fl/−) or two (fl/+) functional copies of Dab2, with a clear effect of gene dosage on expression level. In the conditionally null (−/−) animals shown here, neither form of the Dab2 protein was detected, although, in some conditional animals, trace amounts of Dab2fl allele remained and were not analyzed further. The birth and survival of conditional null mice suggest that Dab2 is only required in extra-embryonic tissues for all steps of normal development. This is consistent with the embryonic lethality due to defective AVE induction, and further suggests that Nodal signaling in the epiblast is independent of Dab2. Figure 7.Rescue of Dab2-deficient mice with Meox2–Cre. (A) Morphology of E11.5 embryos with either one functional copy of Dab2 (Dab2fl/−) or conditionally null for Dab2 (Dab2fl/−; Meox2cre/+). (B) PCR analysis of P8 pups (tag number 2148–2153) born from a Dab2fl/fl × Dab2+/−; Meox2cre/+ mating. The upper panel shows the Dab2 genotype, while the lower panel shows the Meox2–Cre genotype. The bottom labels indicate the genotype before and after Cre expression. (C) Immunoblot analysis of protein lysates made from the tails of mice with the genotypes indicated in (B). Forty micrograms of total protein were resolved by 10% SDS–PAGE and immunoblotted with mouse anti-Dab2 antibodies, which recognize the N-terminus common to all known Dab2 isoforms. To verify equal loading, the blot was stripped and reprobed with mouse anti-β-tubulin antibodies. Download figure Download PowerPoint Mice conditionally null for Dab2 exhibit defects in kidney function Dab2 conditionally null animals appear healthy and grow as rapidly as their littermates (data not shown). Moreover, female Dab2−/− mice breed and raise pups. Since Dab2 is highly expressed in a number of adult tissues, including the kidney, ovary, liver, mammary gland, intestine, uterus and heart (Fazili et al., 1999), various organs from Dab2 conditionally null mice were analyzed. Intestinal epithelium from wild-type mice expresses high levels of Dab2, yet the intestinal epithelium from Dab2 conditionally null mice appeared normal (data not shown). The kidney also appeared grossly normal, despite the absence of Dab2 protein that is normally expressed in the kidney proximal tubule (KPT) cells (Figure 8A–D). Figure 8.Analysis of an adult kidney. (A) Immunoblot analysis of adult kidneys of the indicated genotypes. Kidney extracts (7 μg protein) were resolved on a 4–15% SDS–PAGE gradient gel and immunoblotted with mouse anti-Dab2 antibodies. (B–D) Immunohistochemistry of Dab2 localization in kidney. (B) Wild-type kidney, anti-Dab2. (C) Wild-type kidney, control antibody. (D) Conditionally null kidney, anti-Dab2. Note specific staining in the proximal tubule (arrows) and non-specific staining in the capillary knot of glomerulus. (E and F) EM of cross- sections through a KPT from a wild-type (E) and conditionally null (F) mouse. Bar = 1 μm. mv, microvilli; E, endosome; M, mitochondria; (arrow) endocytic vesicle; arrowhead, dense apical tubule. Download figure Download PowerPoint Because Dab2 complexes with megalin (Oleinikov et al., 2000), we examined kidney function. Megalin is highly expressed in the KPT, where it is important for the reabsorption of several plasma proteins from the primary filtrate (Christensen and Birn, 2001). As a result, megalin−/− mice secrete excess quantities of vitamin D binding protein (DBP) (Nykjaer et al., 1999) and retinol binding protein (RBP) (Christensen and Willnow, 1999) in the urine, and megalin−/− KPT cells have reduced numbers of clathrin-coated pits and vesicles (Willnow et al., 1996; Nykjaer et al., 1999). EM showed that Dab2 deletion does not reduce the apical microvilli or junctional complexes between KPT cells, but the number of coated pits and endocytic vesicles near the apical membrane was significantly reduced as compared with wild type (Figure 8E and F). This suggests possible changes in transport of molecules from the apical surface of the KPT cells. Urine was collected from Dab2fl/+, Dab2fl/− and Dab2−/− mice and analyzed for DBP, RBP and other proteins (Figure 9). While wild-type and heterozygous animals did not excrete DBP (Figure 9A, lanes 3–6 and 9–12), the urine of male and female conditionally null mice contained DBP (Figure 9A, lanes 1 and 2 and 7 and 8). Increased excretion of DBP was not a consequence of increased DBP levels in the plasma, since plasma DBP levels were unchanged (Figure 9B). Similarly, the urine of male and female conditionally null mice contained RBP (Figure 9C). Silver staining of gels also revealed increased levels of other proteins in Dab2−/− urine (Figure 9D), although total protein content and the level of the major urinary protein (MUP), a protein whose reabsorption is not dependent on megalin, were not systematically altered (Figure 9E). Interestingly, both the defect in DBP and RBP reabsorption, and the reduction in apical clathrin-coated pits, reflect the phenotypes reported for megalin-deficient mice (Christensen and Willnow, 1999; Nykjaer et al., 1999). Figure 9.Urine and plasma analysis of Dab2 conditionally null mice. (A) Urine samples (15 μg protein) were resolved by 12.5% SDS–PAGE and immunoblotted with rabbit anti-DBP antibodies. (B) Plasma (0.5 μl) obtained from the same mice was immunoblotted with rabbit anti-DBP antibodies. (C) Urine protein (15 μg) was resolved by 15% SDS–PAGE and immunoblotted with sheep anti-RBP antibodies. (D) Urine protein (1.5 μg) was resolved by 15% SDS–PAGE and silver stained. Asterisks indicate proteins that were increased in urine from conditionally null mice. (E) Urine protein (1.5 μg) was subjected to 15% SDS–PAGE and stained with Coommassie Blue to detect the secreted levels of the major urinary protein (MUP). Download figure Download PowerPoint Discussion Our genetic analysis shows that Dab2 is required for normal embryonic VE development and also facilitates a transport process in an adult epithelium. Embryos lacking Dab2 are able to implant, but they fail to gastrulate and cease developing around E6.0–6.5. The localization of Dab2 expression to the VE, the rescue of development when Dab2 is supplied in extra-embryonic tissues, the lack of induction of AVE markers, and the failure of Dab2−/− blastocysts to develop normally in vitro, all provide evidence that Dab2 is likely needed for Nodal signaling in the VE. This apparent requirement may be direct or indirect, as discussed below, and Dab2 may have additional functions in the VE that we have not detected. When Dab2 is supplied in extra-embryonic tissues, Dab2−/− embryos are efficiently rescued, implying that Dab2 is not needed for subsequent Nodal or other signaling events in the embryo proper. However, Dab2 is required for normal endocytosis in the proximal tubule cells of the kidney, as shown by the reduced number of apical coated pits and vesicles and increased excretion of DBP, RBP and certain other proteins, linking Dab2 to the megalin-dependent protein trafficking machinery. Dab2 has an essential function in the VE The developmental defects observed in the Dab2−/− embryos resemble some of the phenotypes described in SMAD2 and SMAD4 mutants (Nomura and Li, 1998; Sirard et al., 1998; Waldrip et al., 1998; Weinstein et al., 1998; Yang et al., 1998). These mutants fail to form a primitive streak, the proximal extra-embryonic region of the egg cylinder is truncated, and AVE markers, such as Cerr1 and Hex, are not induced in the distal VE. These phenotypes are rescued by wild-type extra-embryonic cells (Sirard et al., 1998; Waldrip et al., 1998). Thus it is likely that Dab2 is needed in the VE to respond to Nodal coming from the epiblast (Beddington and Robertson, 1999; Lu et al., 2001). However, Dab2 appears not to be needed for Nodal functions in the embryo, such as mesoderm and endoderm induction, A-P axis patterning and establishment of left–right asymmetry (Schier and Shen, 2000), since it is not detectably expressed in the epiblast at E6.5–7.5 and can be deleted without detriment. Induction of specific genes by Nodal is known to depend on different components in different cell types (Ding et al., 1998; Brennan et al., 2001).