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

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
Research Article
Dynamic redistribution of vasa homolog and exclusion of somatic cell determinants during germ cell specification in Ciona intestinalis
Maki Shirae-Kurabayashi, Takahito Nishikata, Katsumi Takamura, Kimio J. Tanaka, Chiaki Nakamoto, Akira Nakamura
Development 2006 133: 2683-2693; doi: 10.1242/dev.02446
Maki Shirae-Kurabayashi
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Takahito Nishikata
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Katsumi Takamura
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Kimio J. Tanaka
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Chiaki Nakamoto
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Akira Nakamura
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Figures & tables
  • Info & metrics
  • PDF
Loading

Article Figures & Tables

Figures

  •     Fig. 1.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 1.

    Expression patterns of CiVH and Ci-PEM RNAs during embryogenesis. (A-G) CiVH RNA expression; (H-N) Ci-PEM RNA expression. Although both Ci-PEM and CiVH RNA localize to the postplasm and to the middle of the tail at the tailbud stage (arrowheads), the CiVH RNA shows a different specific distribution in the posterior region of the tail in tailbud embryos (arrows).

  •     Fig. 2.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 2.

    CiVH protein is localized to two discrete regions through the B7.6 cell division. Embryos were stained for CiVH protein (green) and for F-actin (magenta) to visualize the cell boundary. A-C, dorsal views; E-G, lateral views. Anterior is towards the left in all panels. (A,B) CiVH protein (green) accumulated at the posterior cortex of the B7.6 cells with an F-actin layer (A′,B′, arrowheads). (A″,B″) Phalloidin staining alone highlights a thick layer of cortical F-actin in the CAB region (arrowheads). (C,C′) At the mid-gastrula stage, while some CiVH protein remained associated with an F-actin mass (C′, arrowhead), some was diffused in the cytoplasm of the B7.6 cells (C′, arrows). Diagrams show the position of the B7.6 cells in above embryos (upper row; outlined in red) and distribution of CiVH protein within the B7.6 cells (lower row; red). (D) A mid-gastrula embryo showing the pH3-positive chromosomes in one of the B7.6 cells (D′, yellow). pH3-positive chromosomes are aligned, indicating that this pH3-positive B7.6 cell was in metaphase (arrow). (E-G) In the B8.11 cells (E′,F′,G′, arrowheads), the CiVH signals were faint. By contrast, the CiVH protein was upregulated in the B8.12 cells (E,F, arrows), forming CiVH granules in the cytoplasm (E′,F′ arrows). (G) The B8.12 cells divided to form four CiVH-positive cells at the late-tailbud stage (arrows in G,G‴). These cells formed perinuclear CiVH granules (arrows in G‴). (G″) Phalloidin staining alone highlighting the F-actin aggregates in the B8.11 cells (arrowhead). Diagrams show the positions of CiVH-positive B7.6 descendants in above embryos.

  •     Fig. 3.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 3.

    CiVH-positive cells in the tail region become germ cells. (A,B) An early tadpole larva. Eight CiVH-positive cells were localized to the distal region of the tail (arrowheads in B). CiVH signals were also detected in the trunk region (arrow). (C) A late tadpole-stage larva. CiVH signals in the trunk were remarkably reduced (arrow). (D) A larva during tail resorption. CiVH-positive cells were found in the tail (arrowhead), and the CiVH signals in the trunk were undetectable. (E) A stage 3a juvenile. CiVH-positive cells were among those in the tail debris (arrowhead). (F,F′) A stage 3b juvenile. CiVH-positive cells (arrowheads) remained among the cells in the tail debris (outlined). (G,G′) A stage 4 juvenile. CiVH-positive cells were aligned within the tail debris, which was almost completely resorbed (outlined). (H,H′) A stage 5 juvenile. CiVH-positive cells (arrowheads) were aligned within the tube-like structure. (I,I′) A stage 6 juvenile. CiVH-positive cells (arrowhead) changed position within the tube to form a drop-like cluster. (J,J′) A stage 7 juvenile. The CiVH-positive cells (arrowheads) were entirely surrounded by somatic tissue. The number of CiVH-positive cells in the gonad increased.

  •     Fig. 4.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 4.

    B8.12 descendants coalesce into the gonad. (A) A gastrula embryo with DiI-labeled B7.6 cells (arrowhead). (B) A tailbud embryo with DiI signals in the B8.11 (arrowhead) and B8.12 (arrow) cells. (C) A stage 6 juvenile, in which the B7.6 cells were DiI labeled, were stained for CiVH (green). The arrowhead indicates the primitive gonads. Five DiI-labeled cells (arrowheads) that were also CiVH positive coalesced into the gonads (inset). (D) A larva in which B7.6 blastomeres were DiI-labeled and the distal part of the tail containing the B8.12 descendants was cut off. The DiI signals remained in the B8.11 cells of the tail (arrowhead). (E) A stage 5 tail-cut juvenile. The DiI-positive B8.11 cells were present on the gut wall (arrowhead). Owing to the capture of a faint DiI signal, the auto-fluorescence from the tail debris was relatively prominent (arrow). No CiVH-positive cells were detected in this juvenile (data not shown).

  •     Fig. 5.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 5.

    CiVH RNA and protein are inherited by the B8.12 cells through their release from the CAB. Embryos were stained for CiVH protein (magenta) and CiVH RNA (green), and their nuclei were labeled (blue in J,O). (A-E) A 32-cell stage embryo; (F-J) a gastrula embryo; (K-O) a mid-tailbud embryo. (B-E,G-J,L-O) Enlarged views of A,F,K. (A,B,F,G,K,L) Nomarski optics. (C-E) CiVH protein and RNA concentrated to the CAB during cleavage stages (arrowheads). (H-J) Some CiVH protein (white arrows) and RNA (yellow arrows) diffused together from the CAB (arrowheads) in gastrula stage embryos. (M-O) In tailbud embryos, although CiVH protein and RNA colocalized in the B8.11 cells (arrowheads), they were separated in the cytoplasm within the B8.12 cells (white and yellow arrows, respectively).

  •     Fig. 6.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 6.

    Ci-PEM RNA and CiVH protein show different distributions after the gastrula stage. Embryos were stained for CiVH protein (magenta) and for Ci-PEM RNA (green). Nuclei were labeled in blue (J,O). (A-E) A 32-cell stage embryo; (F-J) a gastrula embryo; (K-O) a tailbud embryo. (B-E,G-J,L-O) Enlarged views of A,F,K. (A,B,F,G,K,L) Nomarski optics. Although the CiVH protein was released from the CAB and diffused into the cytoplasm (H,J, arrows), the Ci-PEM RNA remained in the anterior-most region in the B7.6 cells at the gastrula stage (I,J, arrowheads), resulting in its inheritance only by the B8.11 cells at the tailbud stage (N,O, arrowheads).

  •     Fig. 7.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 7.

    CiYB1 protein is inherited only by the B8.11 cells, along with Ci-PEM RNA. Embryos were stained for CiYB1 protein (magenta) and Ci-REM RNA (green). (A-E) A 32-cell embryo; (F-J) a gastrula embryo; (K-O) a mid-tailbud embryo. (B-E,G-J, L-O) Enlarged views of A,F,K. (A,B,F,G,K,L) Nomarski optics. The CiYB1 protein tightly colocalized with Ci-PEM RNA and segregated only into the B8.11 cells (E,J,O).

  •     Fig. 8.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 8.

    CiVH protein production in the B8.12 cells depends on the translation of maternally inherited RNA. (A,A′) Untreated mid-tailbud-stage embryos, showing CiVH signals in the B8.11 (arrowhead) and B8.12 (arrow) cells. (B,B′) AcD-treated embryos. Although the treatment severely affected embryogenesis, strong CiVH signals were detected in the presumptive B8.11 (arrowhead) and B8.12 (arrow) cells. (C,C′) Puromycin-treated embryos, in which CiVH signals in the presumptive B8.12 cells were almost undetectable. Owing to the capture of a faint CiVH signals (C′ arrow), background signals in the cortical rim were relatively prominent. (A″,B″,C″) Histochemical staining for AP activity under each condition. (D) Expression of Ci-AP, CiVH and β-tubulin RNAs, analyzed by RT-PCR. A severe reduction in the expression of Ci-AP mRNA in the AcD-treated embryos was confirmed by using two different primer sets (AP-1, AP-2). The negative controls without reverse transcriptase (RT) are shown in the lanes (-) to the left of each RT-positive lane (+).

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.
Dynamic redistribution of vasa homolog and exclusion of somatic cell determinants during germ cell specification in Ciona intestinalis
(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
Research Article
Dynamic redistribution of vasa homolog and exclusion of somatic cell determinants during germ cell specification in Ciona intestinalis
Maki Shirae-Kurabayashi, Takahito Nishikata, Katsumi Takamura, Kimio J. Tanaka, Chiaki Nakamoto, Akira Nakamura
Development 2006 133: 2683-2693; doi: 10.1242/dev.02446
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
Citation Tools
Research Article
Dynamic redistribution of vasa homolog and exclusion of somatic cell determinants during germ cell specification in Ciona intestinalis
Maki Shirae-Kurabayashi, Takahito Nishikata, Katsumi Takamura, Kimio J. Tanaka, Chiaki Nakamoto, Akira Nakamura
Development 2006 133: 2683-2693; doi: 10.1242/dev.02446

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
    • Summary
    • INTRODUCTION
    • MATERIALS AND METHODS
    • RESULTS
    • DISCUSSION
    • Acknowledgments
    • Footnotes
    • References
  • Figures & tables
  • Info & metrics
  • PDF

Related articles

Cited by...

More in this TOC section

  • Ror2-mediated non-canonical Wnt signaling regulates Cdc42 and cell proliferation during tooth root development
  • Extensive nuclear gyration and pervasive non-genic transcription during primordial germ cell development in zebrafish
  • Deciphering and modelling the TGF-β signalling interplays specifying the dorsal-ventral axis of the sea urchin embryo
Show more RESEARCH ARTICLES

Similar articles

Other journals from The Company of Biologists

Journal of Cell Science

Journal of Experimental Biology

Disease Models & Mechanisms

Biology Open

Advertisement

Kathryn Virginia Anderson (1952-2020)

Developmental geneticist Kathryn Anderson passed away at home on 30 November 2020. Tamara Caspary, a former postdoc and friend, remembers Kathryn and her remarkable contribution to developmental biology.


Zooming into 2021

In a new Editorial, Editor-in-Chief James Briscoe and Executive Editor Katherine Brown reflect on the triumphs and tribulations of the last 12 months, and look towards a hopefully calmer and more predictable year.


Read & Publish participation extends worldwide

Over 60 institutions in 12 countries are now participating in our Read & Publish initiative. Here, James Briscoe explains what this means for his institution, The Francis Crick Institute. 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. Sign up to join our next session:

10 February
Time: 13:00 (GMT)
Chaired by: preLights

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