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  • The dynamic right-to-left translocation of Cerl2 is involved in the regulation and termination of nodal activity in the mouse node
    Publication . Inacio, Jose Manuel; Marques, Sara; Nakamura, Tetsuya; Shinohara, Kyosuke; Meno, Chikara; Hamada, Hiroshi; Belo, Jose Antonio
    The determination of left-right body asymmetry in mouse embryos depends on the interplay of molecules In a highly sensitive structure, the node. Here, we show that the localization of Cerl2 protein does not correlate to its mRNA expression pattern, from 3-somite stage onwards. Instead, Cerl2 protein displays a nodal flow-dependent dynamic behavior that controls the activity of Nodal in the node, and the transmission of the laterality information to the left lateral plate mesoderm (LPM). Our results indicate that Cerl2 initially localizes and prevents the activation of Nodal genetic circuitry on the right side of the embryo, and later its right-to-left translocation shutdowns Nodal activity in the node. The consequent prolonged Nodal activity in the node by the absence of Cerl2 affects local Nodal expression and prolongs its expression in the LPM. Simultaneous genetic removal of both Nodal node inhibitors, Cerl2 and Lefty1, sustains even longer and bilateral his LPM expression.
  • Targeted Inactivation of Cerberus Like-2 Leads to Left Ventricular Cardiac Hyperplasia and Systolic Dysfunction in the Mouse
    Publication . Araújo, Ana Carolina; Marques, Sara; Belo, José A.
    Previous analysis of the Cerberus like 2 knockout (Cerl2(-/-)) mouse revealed a significant mortality during the first day after birth, mostly due to cardiac defects apparently associated with randomization of the left-right axis. We have however, identified Cerl2-associated cardiac defects, particularly a large increase in the left ventricular myocardial wall in neonates that cannot be explained by laterality abnormalities. Therefore, in order to access the endogenous role of Cerl2 in cardiogenesis, we analyzed the embryonic and neonatal hearts of Cerl2 null mutants that did not display a laterality phenotype. Neonatal mutants obtained from the compound mouse line Cer2(-/-)
  • Generating asymmetries in the early vertebrate embryo: the role of the Cerberus-like family
    Publication . Belo, José A.; Silva, Ana C.; Borges, Ana; Filipe, Mário; Bento, Margaret; Gonçalves, Lisa; Vitorino, Marta; Salgueiro, Ana Marisa; Texeira, Vera; Tavares, Ana T.; Marques, Sara
    One fundamental aspect of vertebrate embryonic development is the formation of the body plan. For this process, asymmetries have to be generated during early stages of development along the three main body axes: Anterior-Posterior, Dorso-Ventral and Left-Right. We have been studying the role of a novel class of molecules,the Cerberus/Dan gene family. These are dedicated secreted antagonists of three major signaling pathways: Nodal, BMP and Wnt. Our studies contribute to the current view that the fine tuning of signaling is controlled by a set of inhibitory molecules rather than by activators. In this context, the Cerberus-like molecules emerge as key players in the regulation and generation of asymmetries in the early vertebrate embryo.
  • Reversal of left-right asymmetry induced by aberrant nodal signaling in the node of mouse embryos
    Publication . Oki, Shinya; Kitajima, Keiko; Marques, Sara; Belo, José A.; Yokoyama, Takahiko; Hamada, Hiroshi; Meno, Chikara
    The node at the anterior tip of the primitive streak serves as an initial generator of the left-right (L-R) axis in mammalian embryos. We now show that a small disturbance in molecular signaling at the node is responsible for the L-R reversal of visceral organs in the inv mutant mouse. In the node of wild-type embryos, the expression of Nodal and Cerl2 (Dand5), which encodes an inhibitor of Nodal, is asymmetric, with the level of Nodal expression being higher on the left side and that of Cerl2 expression higher on the right. In inv/inv embryos, however, a localized reduction in the level of Cerl2 expression results in upregulation of the Nodal signal and a consequent induction of Lefty expression in the node. The ectopic expression of Lefty1 delays the onset of Nodal expression in the lateral plate mesoderm. L-R asymmetry of Cerl2 expression in the node also becomes reversed in a manner dependent on the Nodal signal. Nodal expression in the lateral plate mesoderm then appears on the right side, probably reflecting the balance between Nodal and Cerl2 in the node. The inhibition of Cerl2 expression by the Nodal signal suggests a mechanism for amplification of the cue for L-R asymmetry provided by nodal flow and for stabilization of asymmetric gene expression around the node. In inv/inv embryos, this system may function in reverse as a result of ectopic production of Lefty, which inhibits the Nodal signal on the left side in a manner dependent on leftward nodal flow.
  • The activity of the Nodal antagonist Cerl-2 in the mouse node is required for correct L/R body axis
    Publication . Marques, Sara; Borges, Ana; Silva, Ana Cristina; Freitas, Sandra; Cordenonsi, M.; Belo, José A.
    Correct establishment of the left/right (L/R) body asymmetry in the mouse embryo requires asymmetric activation of the evolutionarily conserved Nodal signaling cascade in the left lateral plate mesoderm (L-LPM). Furthermore, the presence of Nodal in the node is essential for its own expression in the L-LPM. Here, we have characterized the function of cerl-2, a novel Nodal antagonist, which displays a unique asymmetric expression on the right side of the mouse node. cerl-2 knockout mice display multiple laterality defects including randomization of the L/R axis. These defects can be partially rescued by removing one nodal allele. Our results demonstrate that Cerl-2 plays a key role in restricting the Nodal signaling pathway toward the left side of the mouse embryo by preventing its activity in the right side.
  • Functional analysis of the mouse Nodal antagonist, Cerl2, during left-right axis formation
    Publication . Inacio, Jose M; Marques, Sara; Belo, José A.
    Although recently our understanding of how the LR asymmetry is generated in vertebrate embryos has seen rapid progress, many important questions remain to be explained. In mouse embryos, the leftward flow of the extra-embryonic fluid in the node cavity, called nodal flow, seems to be the symmetry-breaking event. However, it is not yet know how this flow functions or how the asymmetric signal(s) generated in the node is/are transferred to the lateral plate mesoderm. The mouse gene cerberus-like2(cerl2) encodes a 20-kDa protein with a predicted signal peptide sequence and a cysteine-rich domain (CRD) containing nine cysteines characteristic of the Cerberus/DAN family. Whole-mount in situ hybridization studies showed that cerl2 transcripts could be first detected in a horseshoe-shaped expression pattern in the perinodal region of the mouse embryo (E7.0), resembling Nodal expression at this stage. At stage E7.5, expression of cerl2 begins to decrease in intensity on the left side, and by early somitogenesis (E8.0), it can be strongly detected in the right side of the node, assuming a complementary expression pattern to that observed in Nodal. Furthermore, it was shown that Cerl2 activity is upstream of the Nodal receptor inhibiting Nodal and its downstream targets. A physical interaction between these two proteins exists, which suggests that Cerl2 is a secreted Nodal antagonist. Here, to elucidate the role of Cerl2 protein in the early events of symmetry breaking the functional activity of this Nodal antagonist will be discussed.
  • Identification and functional analysis of novel genes expressed in the Anterior Visceral Endoderm
    Publication . Gonçalves Dias Da Silva, Lisa; Filipe, Mario; Marques, Sara; Salgueiro, Ana Marisa; Becker, Jorg D.; Belo, José A.
    During early vertebrate development, the correct establishment of the body axes is critical. The anterior pole of the mouse embryo is established when Distal Visceral Endoderm (DVE) cells migrate to form the Anterior Visceral Endoderm (AVE). Symmetrical expression of Lefty1, Cer1 and Dkk1 determines the direction of DVE migration and the future anterior side. In addition to the establishment of the Anterior-Posterior axis, the AVE has also been implicated in anterior neural specification. To better understand the role of the AVE in these processes, we have performed a differential screening using Affymetrix GeneChip technology with AVE cells isolated from cer1P-EGFP transgenic mouse embryos. We found 175 genes which were upregulated in the AVE and 36 genes in the Proximal-posterior sample. Using DAVID software, we characterized the AVE cell population regarding cellular component, molecular function and biological processes. Among the genes that were found to be upregulated in the AVE, several novel genes were identified. Four of these transcripts displaying high-fold change in the AVE were further characterized by in situ hybridization in early stages of development in order to validate the screening. From those four selected genes, one, denominated Adtk1, was chosen to be functionally characterized by targeted inactivation in ES cells. Adtk1 encodes for a serine/threonine kinase. Adtk1 null mutants are smaller and present short limbs due to decreased mineralization, suggesting a potential role in chondrogenesis during limb development. Taken together, these data point to the importance of reporting novel genes present in the AVE.
  • Study of Xenopus orthologs of novel genes expressed in the mouse AVE
    Publication . Becker, Jorg D.; Steinbeisser, Herbert; Belo, A.; Silva, Ana C.; Vitorino, Marta; Filipa, Mário; Marques, Sara