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
Identifying targets of the rough homeobox gene of Drosophila: evidence that rhomboid functions in eye development
M. Freeman, B.E. Kimmel, G.M. Rubin
Development 1992 116: 335-346;
M. Freeman
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
B.E. Kimmel
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
G.M. Rubin
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Info & metrics
  • PDF
Loading

Summary

In order to identify potential target genes of the rough homeodomain protein, which is known to specify some aspects of the R2/R5 photoreceptor subtype in the Drosophila eye, we have carried out a search for enhancer trap lines whose expression is rough-dependent. We crossed 101 enhancer traps that are expressed in the developing eye into a rough mutant background, and have identified seven lines that have altered expression patterns. One of these putative rough target genes is rhomboid, a gene known to be required for dorsoventral patterning and development of some of the nervous system in the embryo. We have examined the role of rhomboid in eye development and find that, while mutant clones have only a subtle phenotype, ectopic expression of the gene causes the non-neuronal mystery cells to be transformed into photoreceptors. We propose that rhomboid is a part of a partially redundant network of genes that specify photoreceptor cell fate.

REFERENCES

    1. Affolter M.,
    2. Schier A.,
    3. Gehring W.
    (1990) Homeodomain proteins and the regulation of gene expression. Curr. Opin. Cell Biol 2, 485–495
    OpenUrlCrossRefPubMed
    1. Andrew D. J.,
    2. Scott M. P.
    (1992) Downstream of the homeotic genes. New Biologist 4, 5–15
    OpenUrlPubMedWeb of Science
    1. Baker N. E.,
    2. Mlodzik M.,
    3. Rubin G. M.
    (1990) Spacing differentiation in the developing Drosophila eye: a fibrinogen-related lateral inhibitor encoded by scabrous. Science 250, 1370–1377
    OpenUrlAbstract/FREE Full Text
    1. Basler K.,
    2. Siegrist P.,
    3. Hafen E.
    (1989) The spatial and temporal expression pattern of sevenless is exclusively controlled by gene-internal elements. EMBO J 8, 2381–2386
    OpenUrlPubMedWeb of Science
    1. Basler K.,
    2. Yen D.,
    3. Tomlinson A.,
    4. Hafen E.
    (1990) Reprogramming cell fate in the developing Drosophila retina: transformation of R7 cells by ectopic expression of rough. Genes Dev 4, 728–739
    OpenUrlAbstract/FREE Full Text
    1. Bellen H.,
    2. O'Kane C. J.,
    3. Wilson C.,
    4. Grossniklaus U.,
    5. Kurth-Pearson R.,
    6. Gehring W. J.
    (1989) P-element mediated enhancer detection: a versatile method to study development in Drosophila. Genes Dev 3, 1288–1300
    OpenUrlAbstract/FREE Full Text
    1. Bienz M.,
    2. Tremml G.
    (1988) Domain of Ultrabithorax expression in Drosophila visceral mesoderm from autoregulation and exclusion. Nature 333, 576–578
    OpenUrlCrossRefPubMed
    1. Bier E.,
    2. Jan L. Y.,
    3. Jan Y. N.
    (1990) rhomboid, a gene required for dorsoventral axis establishment and peripheral nervous system development in Drosophila melanogaster. Genes Dev 4, 190–203
    OpenUrlAbstract/FREE Full Text
    1. Bowtell D. D.,
    2. Simon M. A.,
    3. Rubin G. M.
    (1988) Nucleotide sequence and structure of the sevenless gene of Drosophila melanogaster. Genes Dev 2, 620–634
    OpenUrlAbstract/FREE Full Text
    1. Bowtell D. D. L.,
    2. Kimmel B. E.,
    3. Simon M. A.,
    4. Rubin G. M.
    (1989) Regulation of the complex pattern of sevenless expression in the developing Drosophila eye. Proc. Natl. Acad. Sci. USA 86, 6245–6249
    OpenUrlAbstract/FREE Full Text
    1. Daniels S. B.,
    2. McCarron M.,
    3. Love C.,
    4. Chovnick A.
    (1985) Dysgenesis-induced instability of rosy locus transformation in Drosophila melanogaster: analysis of excision events and the selective recovery of control element deletions. Genetics 109, 95–117
    OpenUrlAbstract/FREE Full Text
    1. Fischer-Vize J. A.,
    2. Vize P. D.,
    3. Rubin G. M.
    (1992) A unique mutation in the Enhancer of split complex affects the fates of the mystery cells in the developing Drosophila eye disc. Development 115, 89–101
    OpenUrlAbstract
    1. Freeman M.
    (1991) First, trap your enhancer. Curr. Biol 1, 378–381
    OpenUrlCrossRefPubMed
    1. Freeman M.,
    2. Klämbt C.,
    3. Goodman C. S.,
    4. Rubin G. M.
    (1992) The argos gene encodes a diffusible factor that regulates cell fate decisions in the Drosophila eye. Cell, 69, 963–975
    OpenUrlCrossRefPubMedWeb of Science
    1. Hafen E.,
    2. Levine M.,
    3. Gehring W. J.
    (1984) Regulation of Antennapedia transcript distribution by the bithorax complex in Drosophila. Nature 307, 287–289
    OpenUrlCrossRefPubMed
    1. Hall L. M. C.,
    2. Mason P. J.,
    3. Spierer P.
    (1983) Transcripts, genes and bands in 315,000 base-pairs of Drosophila DNA. J. Mol. Biol 169, 83–96
    OpenUrlCrossRefPubMedWeb of Science
    1. Hayashi S.,
    2. Scott M. P.
    (1990) What determines the specificity of action of Drosophila homeodomain proteins?. Cell 63, 883–894
    OpenUrlCrossRefPubMedWeb of Science
    1. Heberlein U.,
    2. Mlodzik M.,
    3. Rubin G. M.
    (1991) Cell-fate determination in the developing Drosophila eye: role of the rough gene. Development 112, 703–712
    OpenUrlAbstract
    1. Heberlein U.,
    2. Rubin G. M.
    (1991) Star is required in a subset of photoreceptor cells in the developing Drosophila retina and displays dosage sensitive interactions with rough. Dev. Biol 144, 353–361
    OpenUrlCrossRefPubMedWeb of Science
    1. Hortsch M.,
    2. Bieber A. J.,
    3. Patel N. H.,
    4. Goodman C. S.
    (1990) Differential splicing generates a nervous system-specific form of Drosophila neuroglian. Neuron 4, 697–709
    OpenUrlCrossRefPubMedWeb of Science
    1. Ingolia T. D.,
    2. Craig E. A.,
    3. McCarthy B. J.
    (1980) Sequence of three copies of the gene for the major Drosophila heat shock induced protein and their flanking regions. Cell 21, 669–679
    OpenUrlCrossRefPubMedWeb of Science
    1. Kimmel B. E.,
    2. Heberlein U.,
    3. Rubin G. M.
    (1990) The homeodomain protein rough is expressed in a subset of cells in the developing Drosophila eye where it can specify photoreceptor cell subtype. Genes Dev 4, 712–727
    OpenUrlAbstract/FREE Full Text
    1. Klemenz R.,
    2. Weber U.,
    3. Gehring W. J.
    (1987) The white gene as a marker in a new P-element vector for gene transfer in Drosophila. Nucleic. Acids. Res 15, 3947–3959
    OpenUrlAbstract/FREE Full Text
    1. Koerner T. J.,
    2. Hill J. E.,
    3. Myers A. M.,
    4. Tzagoloff A.
    (1991) High expression vectors with multiple cloning sites for the construction of trpE fusion genes: pATH vectors. Methods Enzymol 194, 477–490
    OpenUrlCrossRefPubMedWeb of Science
    1. Krämer H.,
    2. Cagan R. L.,
    3. Zipursky S. L.
    (1991) Interaction of bride of sevenless membrane-bound ligand and the sevenless tyrosine-kinase receptor. Nature 352, 207–212
    OpenUrlCrossRefPubMedWeb of Science
    1. Mayer U.,
    2. Nusslein-Volhard C.
    (1988) A group of genes required for pattern formation in the ventral ectoderm of the Drosophila embryo. Genes Dev 2, 1496–1511
    OpenUrlAbstract/FREE Full Text
    1. McGinnis W.,
    2. Levine M. S.,
    3. Hafen E.,
    4. Kuroiwa A.,
    5. Gehring W. J.
    (1984) A conserved DNA sequence in homoeotic genes of the Drosophila Antennapedia and bithorax complexes. Nature 308, 428–433
    OpenUrlCrossRefPubMedWeb of Science
    1. Mlodzik M.,
    2. Hiromi Y.,
    3. Weber U.,
    4. Goodman C. S.,
    5. Rubin G. M.
    (1990) The Drosophila seven-up gene, a member of the steroid receptor gene superfamily, controls photoreceptor cell fates. Cell 60, 211–224
    OpenUrlCrossRefPubMedWeb of Science
    1. Ready D.
    (1989) A multifaceted approach to neural development. Trends Neurosci 12, 102–110
    OpenUrlCrossRefPubMedWeb of Science
    1. Reuter R.,
    2. Panganiban G. E. F.,
    3. Hoffmann F. M.,
    4. Scott M. P.
    (1990) Homeotic genes regulate the spatial expression of putative growth factors in the visceral mesoderm of Drosophila embryos. Development 110, 1031–1040
    OpenUrlAbstract/FREE Full Text
    1. Robertson H. M.,
    2. Preston C. R.,
    3. Phillis R. W.,
    4. Johnson-Schlitz D. M.,
    5. Benz W. K.,
    6. Engels W. R.
    (1988) A stable genomic source of P element transposase in Drosophila melanogaster. Genetics 118, 461–470
    OpenUrlAbstract/FREE Full Text
    1. Spradling A. C.,
    2. Rubin G. M.
    (1982) Transposition of cloned P elements into Drosophila germ line chromosomes. Science 218, 341–347
    OpenUrlAbstract/FREE Full Text
    1. Struhl G.,
    2. White R. A.
    (1985) Regulation of the Ultrabithorax gene of Drosophila by other bithorax complex genes. Cell 43, 507–519
    OpenUrlCrossRefPubMedWeb of Science
    1. Tomlinson A.
    (1988) Cellular interactions in the developing Drosophila eye. Development 104, 183–193
    OpenUrlPubMedWeb of Science
    1. Tomlinson A.,
    2. Kimmel B. E.,
    3. Rubin G. M.
    (1988) rough, a346 Drosophila homeobox gene required in photoreceptors R2 and R5 for inductive interactions in the developing eye. Cell 55, 771–784
    OpenUrlCrossRefPubMedWeb of Science
    1. Van den Heuvel M.,
    2. Nusse R.,
    3. Johnston P.,
    4. Lawrence P. A.
    (1989) Distribution of the wingless gene product in Drosophila embryos: a protein involved in cell-cell communication. Cell 59, 739–749
    OpenUrlCrossRefPubMedWeb of Science
    1. Van Vactor D.,
    2. Cagan R.,
    3. Kramer H.,
    4. Zipursky S.
    (1991) Induction in the developing compound eye of Drosophila: Multiple mechanisms restrict R7 induction to a single precursor cell. Cell 67, 1145–1155
    OpenUrlCrossRefPubMedWeb of Science
    1. Wagner-Bernholz J. T.,
    2. Wilson C.,
    3. Gibson G.,
    4. Schuh R.,
    5. Gehring W. J.
    (1991) Identification of target genes of the homeotic gene Antennapedia by enhancer detection. Genes Dev 5, 2467–2480
    OpenUrlAbstract/FREE Full Text
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.
Identifying targets of the rough homeobox gene of Drosophila: evidence that rhomboid functions in eye development
(Your Name) has sent you a message from Development
(Your Name) thought you would like to see the Development web site.
Share
JOURNAL ARTICLES
Identifying targets of the rough homeobox gene of Drosophila: evidence that rhomboid functions in eye development
M. Freeman, B.E. Kimmel, G.M. Rubin
Development 1992 116: 335-346;
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
Citation Tools
JOURNAL ARTICLES
Identifying targets of the rough homeobox gene of Drosophila: evidence that rhomboid functions in eye development
M. Freeman, B.E. Kimmel, G.M. Rubin
Development 1992 116: 335-346;

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

  • Non-imprinted Igf2r expression decreases growth and rescues the Tme mutation in mice
  • The dermomyotome dorsomedial lip drives growth and morphogenesis of both the primary myotome and dermomyotome epithelium
  • REF-1, a protein with two bHLH domains, alters the pattern of cell fusion in C. elegans by regulating Hox protein activity
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

The people behind the papers – George Britton and Aryeh Warmflash

George and Aryeh

First author George Britton and his supervisor Aryeh Warmflash discuss their new Development paper in which they apply advanced in vitro culturing techniques to investigate embryonic ectoderm patterning.


Travelling Fellowship – New imaging approach unveils a bigger picture

Highlights from Travelling Fellowship trips

Find out how Pamela Imperadore’s Travelling Fellowship grant from The Company of Biologists took her to Germany, where she used new imaging techniques to investigate the cellular machinery underlying octopus arm regeneration. Don’t miss the next application deadline for 2020 travel, coming up on 29 November. Where will your research take you?


Primer – Principles and applications of optogenetics in developmental biology

Schematic demonstrating the approaches to controlling protein activity using optogenetics.

Protein function can be controlled by light using optogenetic techniques. In their new Primer, Stefano De Renzis and his colleagues in Heidelberg provide an overview of the most commonly used optogenetic tools and their application in developmental biology.


preLights – Self-organised symmetry breaking in zebrafish reveals feedback from morphogenesis to pattern formation

Sundar Naganathan

preLighter Sundar Naganathan explains his selected preprint by Vikas Trivedi, Benjamin Steventon and their co-workers on pescoids, a new in vitro model system to study early zebrafish embryogenesis.


Spotlight – Can laboratory model systems instruct human limb regeneration?

An extract from a schematic demonstrating the possible pipeline for how discovery in lab model systems can influence applications for regenerative therapies.

One of the most challenging objectives of tissue regeneration research is regrowth of a lost or amputated limb. Here, Ben Cox, Maximina Yun and Kenneth Poss outline the research avenues yet to be explored to move closer to this capstone achievement.


Articles of interest in our sister journals

Tox4 modulates cell fate reprogramming

Lotte Vanheer, Juan Song, Natalie De Geest, Adrian Janiszewski, Irene Talon, Caterina Provenzano, Taeho Oh, Joel Chappell, Vincent Pasque
Journal of Cell Science

Drosophila melanogaster: a simple system for understanding complexity

Stephanie E. Mohr, Norbert Perrimon
Disease Models & Mechanisms

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

© 2019   The Company of Biologists Ltd   Registered Charity 277992