Skip to main content
Advertisement

Main menu

  • Home
  • Articles
    • Accepted manuscripts
    • Issue in progress
    • Latest complete issue
    • Issue archive
    • Archive by article type
    • Special issues
    • Subject collections
    • Sign up for alerts
  • About us
    • About Development
    • About the Node
    • Editors and Board
    • Editor biographies
    • Travelling Fellowships
    • Grants and funding
    • Journal Meetings
    • Workshops
    • The Company of Biologists
    • Journal news
  • For authors
    • Submit a manuscript
    • Aims and scope
    • Presubmission enquiries
    • Article types
    • Manuscript preparation
    • Cover suggestions
    • Editorial process
    • Promoting your paper
    • Open Access
    • Biology Open transfer
  • Journal info
    • Journal policies
    • Rights and permissions
    • Media policies
    • Reviewer guide
    • Sign up for alerts
  • Contacts
    • Contacts
    • Subscriptions
    • Feedback
  • COB
    • About The Company of Biologists
    • Development
    • Journal of Cell Science
    • Journal of Experimental Biology
    • Disease Models & Mechanisms
    • Biology Open

User menu

  • Log in
  • Log out

Search

  • Advanced search
Development
  • COB
    • About The Company of Biologists
    • Development
    • Journal of Cell Science
    • Journal of Experimental Biology
    • Disease Models & Mechanisms
    • Biology Open

supporting biologistsinspiring biology

Development

  • Log in
Advanced search

RSS  Twitter  Facebook  YouTube 

  • Home
  • Articles
    • Accepted manuscripts
    • Issue in progress
    • Latest complete issue
    • Issue archive
    • Archive by article type
    • Special issues
    • Subject collections
    • Sign up for alerts
  • About us
    • About Development
    • About the Node
    • Editors and Board
    • Editor biographies
    • Travelling Fellowships
    • Grants and funding
    • Journal Meetings
    • Workshops
    • The Company of Biologists
    • Journal news
  • For authors
    • Submit a manuscript
    • Aims and scope
    • Presubmission enquiries
    • Article types
    • Manuscript preparation
    • Cover suggestions
    • Editorial process
    • Promoting your paper
    • Open Access
    • Biology Open transfer
  • Journal info
    • Journal policies
    • Rights and permissions
    • Media policies
    • Reviewer guide
    • Sign up for alerts
  • Contacts
    • Contacts
    • Subscriptions
    • Feedback
JOURNAL ARTICLES
Pax-6 functions in boundary formation and axon guidance in the embryonic mouse forebrain
G.S. Mastick, N.M. Davis, G.L. Andrew, S.S. Easter
Development 1997 124: 1985-1997;
G.S. Mastick
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
N.M. Davis
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
G.L. Andrew
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
S.S. Easter
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Info & metrics
  • PDF
Loading

Summary

The Pax-6 gene encodes a transcription factor that is expressed in regionally restricted patterns in the developing brain and eye. Here we describe Pax-6 expression in the early forebrain (prosencephalon) on embryonic day 9.5 (E9.5) to E10.5 using both whole-mount in situ hybridization and antibody labeling. We find close correlations between Pax-6+ domains and initial neural patterning, and identify corresponding defects in embryos homozygous for the Pax-6 allele, Small eye (Sey). Pax-6 expression defines the prosencephalon-mesencephalon boundary, and mutant embryos lack this morphological boundary. Markers of the caudal prosencephalon are lost (Pax-6, Lim-1, Gsh-1) and a marker for mesencephalon is expanded rostrally into the prosencephalon (Dbx). We conclude that the caudal prosencephalon (prosomere 1) is at least partially transformed to a mesencephalic fate. This transformation results in a specific deficit of posterior commissure axons. Sey/Sey embryos also exhibit an axon pathfinding defect specific to the first longitudinal tract in the prosencephalon (tpoc, tract of the postoptic commissure). In wild type, tpoc axons fan out upon coming in contact with a superficial patch of Pax-6+ neuron cell bodies. In the mutant, the tpoc axons have normal initial projections, but make dramatic errors where they contact the neuron cell bodies, and fail to pioneer this first tract. Thus Pax-6 is required for local navigational information used by axons passing through its domain of expression. We conclude that Pax-6 plays multiple roles in forebrain patterning, including boundary formation, regional patterning, neuron specification and axon guidance.

REFERENCES

    1. Acampora D.,
    2. Mazan S.,
    3. Lallemand Y.,
    4. Avantaggiato V.,
    5. Maury M.,
    6. Simeone A.,
    7. Brulet P.
    (1995) Forebrain and midbrain regions are deleted in Otx2/ mutants due to a defective anterior neuroectoderm specification during gastrulation. Development 121, 3279–3290
    OpenUrlAbstract
    1. Barnes J. D.,
    2. Crosby J. L.,
    3. Jones M. C.,
    4. Wright C. V. E.,
    5. Hogan B. L. M.
    (1994) Embryonic expression of Lim-1, the mouse homologue of Xenopus Xlim-1, suggests a role in lateral mesoderm differentiation and neurogenesis. Dev. Biol 161, 168–178
    OpenUrlCrossRefPubMedWeb of Science
    1. Bastiani M. J.,
    2. Harrelson A. L.,
    3. Snow P. M.,
    4. Goodman C. S.
    (1987) Expression of fasciclin I and II glycoproteins on subsets of axon pathways during neural development in the grasshopper. Cell 48, 745–755
    OpenUrlCrossRefPubMedWeb of Science
    1. Bergquist H.,
    2. Kallen B.
    (1954) Notes on the early histogenesis and morphogenesis of the central nervous system in vertebrates. J. Comp. Neurol 100, 627–659
    1. Bulfone A.,
    2. Puelles L.,
    3. Porteus M. H.,
    4. Frohman M. A.,
    5. Martin G. R.,
    6. Rubenstein J. L. R.
    (1993) Spatially restricted expression of Dlx-1, Dlx-2 (Tes-1), Gbx-2, and Wnt-3 in the embryonic day 12. 5 mouse forebraindefines potential transverse and longitudinal segmental boundaries. J. Neurosci 13, 3155–3172
    OpenUrlAbstract
    1. Chalepakis G.,
    2. Wijnholds J.,
    3. Giese P.,
    4. Schachner M.,
    5. Gruss P.
    (1994) Characterization of Pax-6 and Hox-1 binding to the promoter region of the neural cell adhesion molecule L1. DNA Cell Biol 13, 891–900
    OpenUrlCrossRefPubMedWeb of Science
    1. Chedotal A.,
    2. Pourquie O.,
    3. Sotelo C.
    (1995) Initial tract formation in the brain of the chick embryo: selective expression of the BEN/SC1/DM-GRASP cell adhesion molecule. Eur. J. Neurosci 7, 198–212
    OpenUrlCrossRefPubMedWeb of Science
    1. Cvekl A.,
    2. Piatigorsky J.
    (1996) Lens development and crystalline gene expression: many roles for Pax-6. BioEssays 18, 621–630
    OpenUrlCrossRefPubMedWeb of Science
    1. Davis J. A.,
    2. Reed R. R.
    (1996) Role of Olf-1 and Pax-6 transcription factors in neurodevelopment. J. Neurosci 16, 5082–5094
    OpenUrlAbstract/FREE Full Text
    1. Dodd J.,
    2. Morton S. B.,
    3. Karagogeos D.,
    4. Yamamoto M.,
    5. Jessell T. M.
    (1988) Spatial regulation of axonal glycoprotein expression on subsets of embryonic spinal neurons. Neuron 1, 105–116
    OpenUrlCrossRefPubMedWeb of Science
    1. Easter S. S.,
    2. Ross L. S., Jr.,
    3. Frankfurter A.
    (1993) Initial tract formation in the mouse brain. J. Neurosci 13, 285–299
    OpenUrlAbstract
    1. Figdor M. C.,
    2. Stern C. D.
    (1993) Segmental organization of embryonic diencephalon. Nature 363, 630–634
    OpenUrlCrossRefPubMed
    1. Fujii T.,
    2. Pichel J. G.,
    3. Taira M.,
    4. Toyoma R.,
    5. Dawid I. B.,
    6. Westphal H.
    (1994) Expression patterns of the murine LIM class homeobox gene lim1 in the developing brain and excretory system. Dev. Dyn 199, 73–83
    OpenUrlCrossRefPubMedWeb of Science
    1. Glaser T.,
    2. Walton D. S.,
    3. Maas R. L.
    (1992) Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene. Nat. Genet 2, 232–239
    OpenUrlCrossRefPubMedWeb of Science
    1. Glaser T.,
    2. Jepeal L.,
    3. Edwards J. G.,
    4. Young S. R.,
    5. Favor J.,
    6. Maas R. L.
    (1994) PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects. Nat. Genet 7, 463–471
    OpenUrlCrossRefPubMedWeb of Science
    1. Goulding M. D.,
    2. Chalepakis G.,
    3. Deutsch U.,
    4. Erselius J.,
    5. Gruss P.
    (1991) Pax-3, a novel murine DNA binding protein expressed during early neurogenesis. EMBO J 10, 1135–1147
    OpenUrlPubMedWeb of Science
    1. Grindley J. C.,
    2. Davidson D. R.,
    3. Hill R. E.
    (1995) The role of Pax-6 in eye and nasal development. Development 121, 1433–1442
    OpenUrlAbstract
    1. Guthrie S.,
    2. Lumsden A.
    (1991) Formation and regeneration of rhombomere boundaries in the developing chick hindbrain. Development 112, 221–229
    OpenUrlAbstract
    1. Guthrie S. C.,
    2. Butcher M.,
    3. Lumsden A.
    (1991) Patterns of cell division and interkinetic nuclear migration in the chick embryo hindbrain. J. Neurobiol 22, 742–754
    OpenUrlCrossRefPubMedWeb of Science
    1. Halder G.,
    2. Callaerts P.,
    3. Gehring W. J.
    (1995) Induction of ectopic eyes by targeted expression of the eyeless gene in Drosophila. Science 267, 1788–1792
    OpenUrlAbstract/FREE Full Text
    1. Hanson I. M.,
    2. Fletcher J. M.,
    3. Jordan T.,
    4. Brown A.,
    5. Taylor D.,
    6. Adams R. J.,
    7. Punnett H. H.,
    8. van Heyningen V.
    (1994) Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly. Nat. Genet 6, 168–173
    OpenUrlCrossRefPubMedWeb of Science
    1. Heyman I.,
    2. Faissner A.,
    3. Lumsden A.
    (1995) Cellular and molecular specializations of rhombomere boundaries. Dev. Dynam 204, 301–315
    OpenUrlCrossRefPubMedWeb of Science
    1. Hill R. E.,
    2. Favor J.,
    3. Hogan B. L.,
    4. Ton C. C.,
    5. Saunders G. F.,
    6. Hanson I. M.,
    7. Prosser J.,
    8. Jordan T.,
    9. Hastie N. D.,
    10. van Heyningen V.
    (1991) Mouse Small eye results from mutations in a paired-like homeobox-containing gene. Nature 354, 522–525
    OpenUrlCrossRefPubMedWeb of Science
    1. Hirth F.,
    2. Therianos S.,
    3. Loop T.,
    4. Gehring W. J.,
    5. Reichert H.,
    6. Furukubo-Tokunaga K.
    (1995) Developmental defects in brain segmentation caused by mutations of the homeobox genes orthodenticle and empty spiracles in Drosophila. Neuron 15, 769–778
    OpenUrlCrossRefPubMedWeb of Science
    1. Hogan B. L.,
    2. Horsburgh G.,
    3. Cohen J.,
    4. Hetherington C. M.,
    5. Fisher G.,
    6. Lyon M. F.
    (1986) Small eyes (Sey): a homozygous lethal mutation on chromosome 2 which affects the differentiation of both lens and nasal placodes in the mouse. J. Embryol. Exp. Morphol 97, 95–110
    OpenUrlPubMedWeb of Science
    1. Jordan T.,
    2. Hanson I.,
    3. Zaletayev D.,
    4. Hodgson S.,
    5. Prosser J.,
    6. Seawright A.,
    7. Hastie N.,
    8. van Heyningen V.
    (1992) The human PAX6 gene is mutated in two patients with aniridia. Nat. Genet 1, 328–332
    OpenUrlCrossRefPubMedWeb of Science
    1. Lee M. K.,
    2. Rebhun L. I.,
    3. Frankfurter A.
    (1990) Posttranslational modification of class III beta-tubulin. Proc. Natl. Acad. Sci. USA 87, 7195–7199
    OpenUrlAbstract/FREE Full Text
    1. Li H.,
    2. Zeitler P. S.,
    3. Valerius M. T.,
    4. Small K.,
    5. Potter S. S.
    (1996) Gsh-1, an orphan Hox gene, is required for normal pituitary development. EMBO J 15, 714–724
    OpenUrlPubMedWeb of Science
    1. Logan C.,
    2. Wizenmann A.,
    3. Drescher U.,
    4. Monschau B.,
    5. Bonhoeffer F.,
    6. Lumsden A.
    (1996) Rostral optic tectum acquires caudal characteristics following ectopic Engrailed expression. Curr. Biol 6, 1006–1014
    OpenUrlCrossRefPubMedWeb of Science
    1. Lu S.,
    2. Bogarad L. D.,
    3. Murtha M. T.,
    4. Ruddle F. H.
    (1992) Expressionpattern of a murine homeobox gene, Dbx, displays extreme spatial restriction in embryonic forebrain and spinal cord. Proc. Natl. Acad. Sci. USA 89, 8053–8057
    OpenUrlAbstract/FREE Full Text
    1. Lumsden A.,
    2. Keynes R.
    (1989) Segmental patterns of neuronal development in the chick hindbrain. Nature 337, 424–428
    OpenUrlCrossRefPubMedWeb of Science
    1. Macdonald R.,
    2. Xu Q.,
    3. Barth K. A.,
    4. Mikkola I.,
    5. Holder N.,
    6. Fjose A.,
    7. Krauss S.,
    8. Wilson S. W.
    (1994) Regulatory gene expression boundaries demarcate sites of neuronal differentiation in the embryonic zebrafish forebrain. Neuron 13, 1039–1053
    OpenUrlCrossRefPubMedWeb of Science
    1. Mark M.,
    2. Lufkin T.,
    3. Vonesch J. L.,
    4. Ruberte E.,
    5. Olivo J. C.,
    6. Dolle P.,
    7. Gorry P.,
    8. Lumsden A.,
    9. Chambon P.
    (1993) Two rhombomeres are altered in Hoxa-1 mutant mice. Development 119, 319–338
    OpenUrlAbstract
    1. Martinez S.,
    2. Geijo E.,
    3. Sanchez-Vives M. V.,
    4. Puelles L.,
    5. Gallego R.
    (1992) Reduced junctional permeability at interrhombomeric boundaries. Development 116, 1069–1076
    OpenUrlAbstract
    1. Mastick G. S.,
    2. Easter S. S., Jr
    (1996) Initial organization of neurons and tracts in the embryonic mouse fore-and midbrain. Dev. Biol 173, 79–94
    OpenUrlCrossRefPubMedWeb of Science
    1. Mastick G. S.,
    2. Fan C. M.,
    3. Tessier-Lavigne M.,
    4. Serbedzija G. N.,
    5. McMahon A. P.,
    6. Easter S. S., Jr
    (1996) Early deletion of neuromeres in Wnt-/ mutant mice: evaluation by morphological and molecular markers. J. Comp. Neurol 374, 246–258
    OpenUrlCrossRefPubMedWeb of Science
    1. Matsuo T.,
    2. Osumi-Yamashita N.,
    3. Noji S.,
    4. Ohuchi H.,
    5. Koyama E.,
    6. Myokai F.,
    7. Matsuo N.,
    8. Taniguchi S.,
    9. Doi H.,
    10. Iseki S.,
    11. et al.
    (1993) A mutation in the Pax-6 gene in rat small eye is associated with impaired migration of midbrain crest cells. Nat. Genet 3, 299–304
    OpenUrlCrossRefPubMedWeb of Science
    1. McConnell S. K.,
    2. Ghosh A.,
    3. Shatz C. J.
    (1989) Subplate neurons pioneer the first axon pathway from the cerebral cortex. Science 245, 978–982
    OpenUrlAbstract/FREE Full Text
    1. McKay I. J.,
    2. Muchamore I.,
    3. Krumlauf R.,
    4. Maden M.,
    5. Lumsden A.,
    6. Lewis J.
    (1994) The kreisler mouse: a hindbrain segmentation mutant that lacks two rhombomeres. Development 120, 2199–2211
    OpenUrlAbstract
    1. McMahon A. P.,
    2. Bradley A.
    (1990) The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain. Cell 62, 1073–1085
    OpenUrlCrossRefPubMedWeb of Science
    1. McMahon A. P.,
    2. Joyner A. L.,
    3. Bradley A.,
    4. McMahon J. A.
    (1992) The midbrain-hindbrain phenotype of Wnt-1/Wnt-1 mice results from stepwise deletion of engrailed-expressing cells by 9. 5 days postcoitum. Cell 69, 581–595
    OpenUrlCrossRefPubMedWeb of Science
    1. Moody S. A.,
    2. Quigg M. S.,
    3. Frankfurter A.
    (1987) Development of the peripheral trigeminal system in the chick revealed by an isotype-specific anti-beta-tubulin monoclonal antibody. J. Comp. Neurol 279, 567–580
    OpenUrl
    1. Parr B. A.,
    2. Shea M. J.,
    3. Vassileva G.,
    4. McMahon A. P.
    (1993) Mouse Wnt genes exhibit discrete domains of expression in the early embryonic CNS and limb buds. Development 119, 247–261
    OpenUrlAbstract
    1. Plaza S.,
    2. Dozier C.,
    3. Saule S.
    (1993) Quail Pax-6 (Pax-QNR) encodes a transcription factor able to bind and transactivate its own promoter. Cell Growth Differ 4, 1041–1050
    OpenUrlAbstract
    1. Price M.,
    2. Lazzaro D.,
    3. Pohl T.,
    4. Mattei M.-G.,
    5. Ruther U.,
    6. Olivo J.-C.,
    7. Duboule D.,
    8. Di Lauro R.
    (1992) Regional expression of the homeobox gene Nkx-2. 2 in the developing mouse forebrain. Neuron 8, 241–255
    OpenUrlCrossRefPubMedWeb of Science
    1. Puelles L.,
    2. Rubenstein J. L. R.
    (1993) Expression patterns of homeobox and other putative regulatory genes in the embryonic mouse forebrain suggest a neuromeric organization. Trends. Neurosci 16, 472–479
    OpenUrlCrossRefPubMedWeb of Science
    1. Quinn J. C.,
    2. West J. D.,
    3. Hill R. E.
    (1996) Multiple functions for Pax6 in mouse eye and nasal development. Genes. Dev 10, 435–446
    OpenUrlAbstract/FREE Full Text
    1. Quiring R.,
    2. Walldorf U.,
    3. Kloter U.,
    4. Gehring W. J.
    (1994) Homology of the eyeless gene of Drosophila to the Small eye gene in mice and Aniridia in humans. Science 265, 785–789
    OpenUrlAbstract/FREE Full Text
    1. Retaux S.,
    2. Harris W. A.
    (1996) Engrailed and retinotectal topography. Trends Neurosci 19, 542–546
    OpenUrlCrossRefPubMedWeb of Science
    1. Rubenstein J. L.,
    2. Puelles L.
    (1994) Homeobox gene expression during development of the vertebrate brain. Curr. Top. Dev. Biol 29, 1–63
    OpenUrlPubMedWeb of Science
    1. Schmahl W.,
    2. Knoedlseder M.,
    3. Favor J.,
    4. Davidson D.
    (1993) Defects of neuronal migration and the pathogenesis of cortical malformations are associated with Small eye(Sey) in the mouse, a point mutation at the Pax-6 -locus. Acta. Neuropathol. (Berl) 86, 126–135
    OpenUrlCrossRefPubMed
    1. Shawlot W.,
    2. Behringer R. R.
    (1995) Requirement for Lim1 in head-organizer function. Nature 374, 425–430
    OpenUrlCrossRefPubMed
    1. Shimamura K.,
    2. Hartigan D. J.,
    3. Martinez S.,
    4. Puelles L.,
    5. Rubenstein J. L. R.
    (1995) Longitudinal organization of the anterior neural plate and neural tube. Development 121, 3923–3933
    OpenUrlAbstract
    1. Stoykova A.,
    2. Gruss P.
    (1994) Roles of Pax -genes in developing and adult brain as suggested by expression patterns. J. Neurosci 14, 1395–1412
    OpenUrlAbstract
    1. Stoykova A.,
    2. Fritsch R.,
    3. Walther C.,
    4. Gruss P.
    (1996) Forebrain patterning defects in Small eye mutant mice. Development 122, 3453–3465
    OpenUrlAbstract
    1. Sundin O. H.,
    2. Eichele G.
    (1990) A homeodomain protein reveals the metameric nature of the developing chick hindbrain. Genes. Dev 4, 1267–1276
    OpenUrlAbstract/FREE Full Text
    1. Thomas K. R.,
    2. Capecchi M. R.
    (1990) Targeted disruption of the murine int-1 proto-oncogene resulting in severe abnormalities in midbrain and cerebellar development. Nature 346, 847–850
    OpenUrlCrossRefPubMedWeb of Science
    1. Ton C. C.,
    2. Miwa H.,
    3. Saunders G. F.
    (1992) Small eye (Sey): cloning and characterization of the murine homolog of the human aniridia gene. Genomics 13, 251–256
    OpenUrlCrossRefPubMedWeb of Science
    1. Valerius M. T.,
    2. Li H.,
    3. Stock J. L.,
    4. Weinstein M.,
    5. Kaur S.,
    6. Singh G.,
    7. Potter S. S.
    (1995) Gsh-1: a novel murine homeobox gene expressed in the central nervous system. Dev. Dyn 203, 337–351
    OpenUrlPubMedWeb of Science
    1. Walther C.,
    2. Gruss P.
    (1991) Pax-6, a murine paired box gene, is expressed in the developing CNS. Development 113, 1435–1449
    OpenUrlAbstract
    1. Wilson S. W.,
    2. Ross L. S.,
    3. Parrett T.,
    4. Easter S. S., Jr
    (1990) The development of a simple scaffold of axon tracts in the brain of the embryonic zebrafish, Brachydanio rerio. Development 108, 121–145
    OpenUrlAbstract
    1. Wilson S. W.,
    2. Placzek M.,
    3. Furley A.
    (1993) Border disputes: do boundaries play a role in growth cone guidance?. Trends Neurosci 16, 316–322
    OpenUrlCrossRefPubMedWeb of Science
    1. Wurst W.,
    2. Auerbach A. B.,
    3. Joyner A. L.
    (1994) Multiple developmental defects in Engrailed-1 mutant mice: an early mid-hindbrain deletion and pattern defects in forelimbs and sternum. Development 120, 2065–2075
    OpenUrlAbstract
Previous ArticleNext Article
Back to top
Previous ArticleNext Article

This Issue

 Download PDF

Email

Thank you for your interest in spreading the word on Development.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Pax-6 functions in boundary formation and axon guidance in the embryonic mouse forebrain
(Your Name) has sent you a message from Development
(Your Name) thought you would like to see the Development web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Share
JOURNAL ARTICLES
Pax-6 functions in boundary formation and axon guidance in the embryonic mouse forebrain
G.S. Mastick, N.M. Davis, G.L. Andrew, S.S. Easter
Development 1997 124: 1985-1997;
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
Citation Tools
JOURNAL ARTICLES
Pax-6 functions in boundary formation and axon guidance in the embryonic mouse forebrain
G.S. Mastick, N.M. Davis, G.L. Andrew, S.S. Easter
Development 1997 124: 1985-1997;

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Alerts

Please log in to add an alert for this article.

Sign in to email alerts with your email address

Article navigation

  • Top
  • Article
  • Info & metrics
  • PDF

Related articles

Cited by...

More in this TOC section

  • Groucho augments the repression of multiple Even skipped target genes in establishing parasegment boundaries
  • Axial skeletal patterning in mice lacking all paralogous group 8 Hox genes
  • Morphogenetic cell movements in the middle region of the dermomyotome dorsomedial lip associated with patterning and growth of the primary epaxial myotome
Show more JOURNAL ARTICLES

Similar articles

Other journals from The Company of Biologists

Journal of Cell Science

Journal of Experimental Biology

Disease Models & Mechanisms

Biology Open

Advertisement

An interview with Swathi Arur

Swathi Arur joined the team at Development as an Academic Editor in 2020. Her lab uses multidisciplinary approaches to understand female germline development and fertility. We met with her over Zoom to hear more about her life, her career and her love for C. elegans.


Jim Wells and Hanna Mikkola join our team of Editors

We are pleased to welcome James (Jim) Wells and Hanna Mikkola to our team of Editors. Jim joins us a new Academic Editor, taking over from Gordan Keller, and Hanna joins our team of Associate Editors. Find out more about their research interests and areas of expertise.


New funding scheme supports sustainable events

As part of our Sustainable Conferencing Initiative, we are pleased to announce funding for organisers that seek to reduce the environmental footprint of their event. The next deadline to apply for a Scientific Meeting grant is 26 March 2021.


Read & Publish participation continues to grow

“I’d heard of Read & Publish deals and knew that many universities, including mine, had signed up to them but I had not previously understood the benefits that these deals bring to authors who work at those universities.”

Professor Sally Lowell (University of Edinburgh) shares her experience of publishing Open Access as part of our growing Read & Publish initiative. We now have over 150 institutions in 15 countries and four library consortia taking part – find out more and view our full list of participating institutions.


Upcoming special issues

Imaging Development, Stem Cells and Regeneration
Submission deadline: 30 March 2021
Publication: mid-2021

The Immune System in Development and Regeneration
Guest editors: Florent Ginhoux and Paul Martin
Submission deadline: 1 September 2021
Publication: Spring 2022

Both special issues welcome Review articles as well as Research articles, and will be widely promoted online and at key global conferences.


Development presents...

Our successful webinar series continues into 2021, with early-career researchers presenting their papers and a chance to virtually network with the developmental biology community afterwards. Here, Brandon Carpenter talks about how inherited histone methylation defines the germline versus soma decision in C. elegans. 

Sign up to join our next session:

10 March
Time: TBC
Chaired by: Thomas Lecuit

Articles

  • Accepted manuscripts
  • Issue in progress
  • Latest complete issue
  • Issue archive
  • Archive by article type
  • Special issues
  • Subject collections
  • Sign up for alerts

About us

  • About Development
  • About the Node
  • Editors and board
  • Editor biographies
  • Travelling Fellowships
  • Grants and funding
  • Journal Meetings
  • Workshops
  • The Company of Biologists

For authors

  • Submit a manuscript
  • Aims and scope
  • Presubmission enquiries
  • Article types
  • Manuscript preparation
  • Cover suggestions
  • Editorial process
  • Promoting your paper
  • Open Access
  • Biology Open transfer

Journal info

  • Journal policies
  • Rights and permissions
  • Media policies
  • Reviewer guide
  • Sign up for alerts

Contact

  • Contact Development
  • Subscriptions
  • Advertising
  • Feedback

 Twitter   YouTube   LinkedIn

© 2021   The Company of Biologists Ltd   Registered Charity 277992