Nodal signaling pathway

The Nodal signaling pathway is a signal transduction pathway important in pattern formation and differentiation during embryo development.[1]

The nodal family of proteins, a subset of the transforming growth factor beta (TGFβ) superfamily, is responsible for mesoendoderm induction, patterning of the nervous system, and determination of dorsal- ventral axis in vertebrate embryos. Activation of the Nodal pathway involves nodal binding to activin and activin-like receptors which leads to phosphorylation of the Smad2. The P-Smad2/Smad4 complex translocates into the nucleus to interact with transcription factors such as FoxH1, p53 and Mixer (Xenopus mix-like endodermal regulator). This will, in turn, lead to induction of target genes such as Nodal, Lefty, the antagonist of nodal Cerberus, and others.[2]

The activation of Nodal pathway induces the transcription of many target genes including of its own, but at the same time, micro-RNAs and other proteins interfere with this positive feedback loop in a negative manner at different points of the pathway.[2][3] This balance of activation and inhibition of the signal is necessary to achieve the precise location, concentration and duration of downstream target genes that have an important role early in development. This article will summarize the role of some of the components that participate positively and negatively in regulation the signaling pathway. Although all the major components of Nodal signaling are evolutionary conserved in almost all vertebrates, the regulation of each component of the pathway sometimes varies according to the species.

History

The nodal gene was originally discovered by Conlon et al. by retroviral mutation in mice which led to the isolation of a gene that interfered with normal mouse gastrulation and embryo development.[4] Further study of this gene by Zhou et al. showed that the nodal genes encode a secreted signaling peptide that was sufficient to induce mesoderm cells in the mouse embryo. This was an important finding as many other factors had been implicated in the formation of mesoderm in Xenopus whereas the difficulty of removal of these factors due to embryonic lethality and maternal contribution of genes had kept the ability to assay the knock out phenotypes elusive.[5] Further studies of nodal signaling in other vertebrates such as Cyclops and Squint in zebrafish proved that nodal signaling is adequate to induce mesoderm in all vertebrates.[2]

Selected components of the pathway

Overview of Nodal signaling pathway. Nodal and its repressor Lefty are both expressed in response to Nodal signaling. The protein expression levels are affected due to the activity of the miR-430 super-family. Once the protein is translated, it has to be processed in the extracellular space by Convertases (Furin and PACE4). Mature Nodal binds to the Activin receptors I and II and the co-receptor Cripto/Criptic and phosphorilates Smad2 /3. These Smads form a complex with Smad4 and enter into the nucleus and with the help of p53, Mixer or FoxH1 activate the transcription of genes involved in mesoderm and endoderm induction. Ectodermin, PPM1A, XFDR and Tgf1 negative regulate the pathway by competing with Smad components or transcription factors. The interaction of Nodal with BMPs (BMP3, BMP7), Lefty or with Cerberus in the outside of the cells affects its capability to bind to the receptors and reactivate the signal.

Lefty

The Lefty proteins, divergent members of the TGFβ superfamily of proteins, act as extracellular antagonists of nodal signaling. Expression studies of the lefty homologue, antivin, in zebrafish show that lefty likely acts as a competitive inhibitor of nodal signaling.[6] Overexpression of lefty leads to a phenotype similar to a nodal knockout while overexpression of the activin (nodal-related protein) receptor or even the receptor extracellular domain can rescue the phenotype. As the induction of lefty is dependent upon nodal expression, lefty acts a classic feedback inhibitor for nodal signaling. Like nodals, all vertebrates have at least one lefty gene while many, such as zebrafish and mouse, have two unique lefty genes.

DAN proteins

DAN proteins, such as Cerberus and Coco in Xenopus and Cerberus-like in mouse, also act as antagonists of nodal signaling. Unlike lefty proteins, DAN proteins bind directly to extracellular nodal proteins and prevent signaling. Further, not all DAN proteins are specific to nodal signaling and will also block bone morphogenetic proteins (BMPs) and, in the case of Cerberus and Coco, Wnt signaling as well.[7] This activity is important in neural development and left-right symmetry as will be discussed later.

BMPs

Lefty and Cerberus are not the only ones to be able to interact in the extracellular space with Nodal, there is biochemical evidence that BMP3 and BMP7 form heterodimers with Nodal, causing mutual inhibition of the involved pathways.[8]

Convertases: furin and PACE4

Nodal mRNA produces an immature protein form of nodal that is cleaved by proteins called convertases in order to generate a mature nodal. The subtilisin-like proprotein convertases (SPC) Furin (Spc1) and PACE4 (Spc4) recognize a specific sequence of the precursor of nodal protein and cleaves it to form the mature nodal ligand.[9] Conversely, the immature form of Nodal is still capable to activate the pathway.[10] During nodal transportation to the extracellular space, the nodal co-receptor captures the nodal precursor in lipid rafts and once in the cell surface, Cripto interacts with the convertases and forms a complex that facilitates the processing of nodal.[11]

EGF-CFC proteins

EGF-CFC proteins are membrane bound extracellular factors that serve as essential cofactor in Nodal signaling and in vertebrate development as a whole. This family of cofactors includes One-eyed Pinhead (oep) in Zebrafish, FRL1 in Xenopus, and Cripto and Criptic in mouse and human. Genetic studies of oep in zebrafish have shown that the knockout of both maternal and zygotic oep leads to a phenotype similar to that of the squint/Cyclops (nodals) knockout. Similarly, over-expression of either the nodal (squint/Cyclops) or oep with the knockout of the other does not show phenotypical differences. This evidence coupled with the data that overexpression of oep shows no phenotype corroborates the role of EGF-CFC as an essential cofactor in Nodal signaling.[12]

Dapper2

In mouse, frog and fish, Dapper2, is a negative regulator of mesoderm formation acting through the down-regulation of the Wnt and TGFβ / nodal signaling pathways. In zebrafish, nodal is known to activate the gene expression of dapper2.[13] In the cell surface Dapper2 tightly binds to the active form of the activin type 1 receptors and targets the receptor for lysosomal degradation. Dapper2 overexpression mimics nodal co-receptor loss of function because nodal signal cannot be transduced and therefore it produces less mesoderm. In the mouse embryo, dpr2 mRNA is located across all the embryo 7.5 days post conception (dpc) however its location changes at 8.5-dpc where it is observed at the prospective somites and by 10-dpc, neural tube, otic vesicle and gut; because Dapper2 and Nodal are expressed in the same region, this suggests that Dapper antagonizes mesoderm induction signals derived from Nodal.[14] Somehow the reduction of activin receptors would lead to the decrease in activity of different TGFb pathways.[13]

Smad

Smad proteins are responsible for transducing nodal signals into the nucleus. The binding of Nodal proteins to activin or activin-like serine/threonine kinase receptors results in the phosphorylation of Smad2. Smad2 will then associate with Smad4 and translocate into the nucleus thereby stimulating transcription of nodal target genes. Evidence has been shown that another Smad, Smad3, can be phosphorylated by activated receptors and may also function as an activator of nodal genes. However, knockout of Smad2 in mice leads to disruption of the formation of the primitive streak. This is not sufficient to knockdown all mesoendodermal genes showing that Smad3 has some overlapping function with Smad2. However, the expression of these genes is ubiquitous in Smad2 KO embryos whereas it is limited in the wild type. Smad3 knockouts do not have a phenotype showing that expression overlap with Smad2 is sufficient normal development.[15]

Molecules affecting nodal activation via smad

Ectodermin negatively regulates the nodal pathway by inhibiting the interaction of Smad4 with other Smads inside the nucleus via the mono-ubiquitination Smad4, this modification allow it to be transported out of the cytoplasm where it can be deubiquitinated by FAM protein, allowing it to form complexes again with other Smads.[16][17] Another negative regulator of the pathway intervening with Smads is PPM1A, a phosphatase that acts with Phospho-Smad2/3 making it inactive.[18] Subsequently, Smad2/3 is transported outside the nucleus with the help of RanBP2.[19]

Transcriptional factors controlling signaling

Smad2/3/4 can associate to different transcription factors such as p53, Mixer and FoxH1 and recognize specific cis-regulatory elements to activate the expression of Nodal target genes at a precise time and location and activate genes required for mesoderm induction. There are some other transcription factors that compete for some of the components of the transcriptional machinery for the activation of Nodal target genes. For instance, Tgif1 and Tgif2 are negative co-regulators that compete for the active form of Smad2, reducing the relative concentration of active Smad2 in the nucleus. In Xenopus, the loss-of-function of Tgf1 and Tgf2 causes the up-regulation of Xnr5 and Xnr6.[20] Another example of transcriptional repressors in frog is XFDL, that binds to p53 obstructing the interaction with the Smad2/3/4 complex.[21]

miRNAs controlling signaling

In vertebrates, the evolutionary conserved family of microRNAs miR-430/427/302 is expressed early in development. It has important roles in controlling mesoderm and endoderm specification, and it does it by regulating the protein expression levels of some Nodal signaling components. This family is composed by the teleost miR-430, the amphibian miR-427 and the mammalian miR-302. In zebra fish the miR-430 inhibits translation of Sqt, Lefty1 and Lefty2, in frogs miR-427 regulate Xnr5, Xnr6b, LeftyA and LeftyB, however in humans embryonic stem cells it has been shown that miR-302 negative regulates the expression of only Lefty1 and Lefty2 but it does not seem down-regulate Nodal protein expression levels.[22]

Nodal signaling in development

Mesoendoderm induction

Multiple studies have established that Nodal signal is required for the induction of most mesodermal and endodermal cell types and Squint/Cyclops knockouts in Zebrafish do not develop notochord, heart, kidneys or even blood.[23] The origin and expression pattern of the nodal signaling proteins differs in different species. Mammalian nodal signaling is initiated ubiquitously in epiblast cells and is maintained by autoregulatory signaling of Wnt3 and limited by the induction of antagonists such as Cerberus-like and lefty.[24] Studies in Xenopus have found that xnr expression (the Xenopus nodal) is induced by VegT at the vegetal pole and nodals spread to the blastula.[25] Xnr expression is stabilized by the presence of β-catenin. This information raises the question of how nodal signaling leads to the induction of both endoderm and mesoderm. The answer comes in form of a gradient of nodal protein. Temporal and spatial differences in nodal signaling will result in different cell fates. With the addition of antagonists and variable range of different nodals, a map of cell fates including both mesoderm and endoderm can be drawn for the embryo.[2] However, it is unclear whether nodal signaling is summated or if cells respond to the amplitude of the signal.[26]

Left-Right Patterning

Human anatomy is asymmetric with the heart located on the left side and the liver on the right. Asymmetry is a feature common to all vertebrates and even paired-symmetric organs such as lungs display asymmetries in the number of lobes. Evidence that nodal signaling is responsible for left-right specification comes from genetic analysis of organisms deficient in left-right specification. These genetic studies led to identification of mutations in components in the nodal signaling pathway such as ActRIIB, Criptic, and FoxH1 in mouse.[27] These studies found that the left-right symmetry is created as a result of nodal antagonist expression on the right side of the embryo which is balanced by nodal upregulating itself on the other half of the embryo. The result is a nodal gradient that is high on the ventral side of the embryo and, through antagonist action, declines as a gradient to the midline.

Neural patterning

As nodal signaling give rise to ectoderm and mesoderm, neuroectoderm formation requires blocking nodal signaling which is accomplished by the expression of nodal antagonist, Cerberus. The role of nodal signaling reemerges later in development when nodal signaling is required to specify ventral cell neural patterning. Loss of function of Cyclops or oep in zebrafish results in cyclopic embryos characterized by a lack of medial floor plate and ventral forebrain.[2] Not all nodals result in the formation of mesoectoderm. Xenopus nodal related 3, (Xnr3) a divergent member of the TGFβ superfamily, induces the expression of the protein, Xbra. The Xbra expression pattern, in correlation the expression pattern another neuroinducer, Xlim-1, result in the patterning of the organizer in Xenopus. This signaling in conjucture with other nodals, noggin, chordin, follistatin and others results in the final patterning of vertebrate central nervous system.[28]

References

  1. ↑ Shen MM (March 2007). "Nodal signaling: developmental roles and regulation". Development. 134 (6): 1023–34. doi:10.1242/dev.000166. PMID 17287255.
  2. 1 2 3 4 5 Schier AF (2003). "Nodal signaling in vertebrate development". Annu. Rev. Cell Dev. Biol. 19: 589–621. doi:10.1146/annurev.cellbio.19.041603.094522. PMID 14570583.
  3. ↑ Schier AF (November 2009). "Nodal morphogens". Cold Spring Harb Perspect Biol. 1 (5): a003459. doi:10.1101/cshperspect.a003459. PMC 2773646Freely accessible. PMID 20066122.
  4. ↑ Conlon FL, Barth KS, Robertson EJ (April 1991). "A novel retrovirally induced embryonic lethal mutation in the mouse: assessment of the developmental fate of embryonic stem cells homozygous for the 413.d proviral integration". Development. 111 (4): 969–81. PMID 1879365.
  5. ↑ Zhou X, Sasaki H, Lowe L, Hogan BL, Kuehn MR (February 1993). "Nodal is a novel TGF-beta-like gene expressed in the mouse node during gastrulation". Nature. 361 (6412): 543–7. doi:10.1038/361543a0. PMID 8429908.
  6. ↑ Thisse C, Thisse B (January 1999). "Antivin, a novel and divergent member of the TGFbeta superfamily, negatively regulates mesoderm induction". Development. 126 (2): 229–40. PMID 9847237.
  7. ↑ Piccolo S, Agius E, Leyns L, Bhattacharyya S, Grunz H, Bouwmeester T, De Robertis EM (February 1999). "The head inducer Cerberus is a multifunctional antagonist of Nodal, BMP and Wnt signals". Nature. 397 (6721): 707–10. doi:10.1038/17820. PMC 2323273Freely accessible. PMID 10067895.
  8. ↑ Yeo C, Whitman M (May 2001). "Nodal signals to Smads through Cripto-dependent and Cripto-independent mechanisms". Mol. Cell. 7 (5): 949–57. doi:10.1016/S1097-2765(01)00249-0. PMID 11389842.
  9. ↑ Beck S, Le Good JA, Guzman M, Ben Haim N, Roy K, Beermann F, Constam DB (December 2002). "Extraembryonic proteases regulate Nodal signalling during gastrulation". Nat. Cell Biol. 4 (12): 981–5. doi:10.1038/ncb890. PMID 12447384.
  10. ↑ Ben-Haim N, Lu C, Guzman-Ayala M, Pescatore L, Mesnard D, Bischofberger M, Naef F, Robertson EJ, Constam DB (September 2006). "The nodal precursor acting via activin receptors induces mesoderm by maintaining a source of its convertases and BMP4". Dev. Cell. 11 (3): 313–23. doi:10.1016/j.devcel.2006.07.005. PMID 16950123.
  11. ↑ Blanchet MH, Le Good JA, Mesnard D, Oorschot V, Baflast S, Minchiotti G, Klumperman J, Constam DB (October 2008). "Cripto recruits Furin and PACE4 and controls Nodal trafficking during proteolytic maturation". EMBO J. 27 (19): 2580–91. doi:10.1038/emboj.2008.174. PMC 2567404Freely accessible. PMID 18772886.
  12. ↑ Shen MM, Schier AF (July 2000). "The EGF-CFC gene family in vertebrate development". Trends Genet. 16 (7): 303–9. doi:10.1016/S0168-9525(00)02006-0. PMID 10858660.
  13. 1 2 Chen YG (January 2009). "Endocytic regulation of TGF-beta signaling". Cell Res. 19 (1): 58–70. doi:10.1038/cr.2008.315. PMID 19050695.
  14. ↑ Su Y, Zhang L, Gao X, Meng F, Wen J, Zhou H, Meng A, Chen YG (March 2007). "The evolutionally conserved activity of Dapper2 in antagonizing TGF-beta signaling". FASEB J. 21 (3): 682–90. doi:10.1096/fj.06-6246com. PMID 17197390.
  15. ↑ Whitman M (November 2001). "Nodal signaling in early vertebrate embryos: themes and variations". Dev. Cell. 1 (5): 605–17. doi:10.1016/S1534-5807(01)00076-4. PMID 11709181.
  16. ↑ Dupont S, Zacchigna L, Cordenonsi M, Soligo S, Adorno M, Rugge M, Piccolo S (April 2005). "Germ-layer specification and control of cell growth by Ectodermin, a Smad4 ubiquitin ligase". Cell. 121 (1): 87–99. doi:10.1016/j.cell.2005.01.033. PMID 15820681.
  17. ↑ Dupont S, Mamidi A, Cordenonsi M, Montagner M, Zacchigna L, Adorno M, Martello G, Stinchfield MJ, Soligo S, Morsut L, Inui M, Moro S, Modena N, Argenton F, Newfeld SJ, Piccolo S (January 2009). "FAM/USP9x, a deubiquitinating enzyme essential for TGFbeta signaling, controls Smad4 monoubiquitination". Cell. 136 (1): 123–35. doi:10.1016/j.cell.2008.10.051. PMID 19135894.
  18. ↑ Lin X, Duan X, Liang YY, Su Y, Wrighton KH, Long J, Hu M, Davis CM, Wang J, Brunicardi FC, Shi Y, Chen YG, Meng A, Feng XH (June 2006). "PPM1A functions as a Smad phosphatase to terminate TGFbeta signaling". Cell. 125 (5): 915–28. doi:10.1016/j.cell.2006.03.044. PMID 16751101.
  19. ↑ Dai F, Lin X, Chang C, Feng XH (March 2009). "Nuclear export of Smad2 and Smad3 by RanBP3 facilitates termination of TGF-beta signaling". Dev. Cell. 16 (3): 345–57. doi:10.1016/j.devcel.2009.01.022. PMC 2676691Freely accessible. PMID 19289081.
  20. ↑ Powers SE, Taniguchi K, Yen W, Melhuish TA, Shen J, Walsh CA, Sutherland AE, Wotton D (January 2010). "Tgif1 and Tgif2 regulate Nodal signaling and are required for gastrulation". Development. 137 (2): 249–59. doi:10.1242/dev.040782. PMC 2799159Freely accessible. PMID 20040491.
  21. ↑ Sasai N, Yakura R, Kamiya D, Nakazawa Y, Sasai Y (May 2008). "Ectodermal factor restricts mesoderm differentiation by inhibiting p53". Cell. 133 (5): 878–90. doi:10.1016/j.cell.2008.03.035. PMID 18510931.
  22. ↑ Rosa A, Spagnoli FM, Brivanlou AH (April 2009). "The miR-430/427/302 family controls mesendodermal fate specification via species-specific target selection". Dev. Cell. 16 (4): 517–27. doi:10.1016/j.devcel.2009.02.007. PMID 19386261.
  23. ↑ Gritsman K, Talbot WS, Schier AF (March 2000). "Nodal signaling patterns the organizer". Development. 127 (5): 921–32. PMID 10662632.
  24. ↑ Brennan J, Lu CC, Norris DP, Rodriguez TA, Beddington RS, Robertson EJ (June 2001). "Nodal signalling in the epiblast patterns the early mouse embryo". Nature. 411 (6840): 965–9. doi:10.1038/35082103. PMID 11418863.
  25. ↑ Kofron M, Demel T, Xanthos J, Lohr J, Sun B, Sive H, Osada S, Wright C, Wylie C, Heasman J (December 1999). "Mesoderm induction in Xenopus is a zygotic event regulated by maternal VegT via TGFbeta growth factors". Development. 126 (24): 5759–70. PMID 10572051.
  26. ↑ Green J (December 2002). "Morphogen gradients, positional information, and Xenopus: interplay of theory and experiment". Dev. Dyn. 225 (4): 392–408. doi:10.1002/dvdy.10170. PMID 12454918.
  27. ↑ Burdine RD, Schier AF (April 2000). "Conserved and divergent mechanisms in left-right axis formation". Genes Dev. 14 (7): 763–76. PMID 10766733.
  28. ↑ Taira M, Saint-Jeannet JP, Dawid IB (February 1997). "Role of the Xlim-1 and Xbra genes in anteroposterior patterning of neural tissue by the head and trunk organizer". Proc. Natl. Acad. Sci. U.S.A. 94 (3): 895–900. doi:10.1073/pnas.94.3.895. PMC 19610Freely accessible. PMID 9023353.

Further reading

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