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A) <t>Ciona</t> <t>robusta</t> (intestinalis type A) embryo at Hotta Stage 25 (late tailbud III, ∼13 hours post-fertilization at 20°C), showing cell outlines and the oral siphon placode (OSP) rosette revealed by Phalloidin-AlexFluor546 staining. B ) In situ mRNA hybridization revealing Protocadherin.e ( Pcdh.e ) expression in the presumptive OSP, as well as in the Motor Ganglion Interneuron 2 (MGIN2) cells as previously reported . C ) Summary diagram of the separation of Six1/2+, future Protocadherin.e (Pcdh.e)- and Pitx- expressing oral siphon placode cells (red outline) from other Foxc+ cells (blue), mainly those contributing to the papillae. D ) Protein domain analysis diagram of Protocadherin.e (Pcdh.e) from SMART , showing presence of a signal peptide (red block), 6 extracellular cadherin repeats (CA) and a transmembrane (TM) domain, similar to the organization of vertebrate protocadherin-family proteins.
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A) <t>Ciona</t> <t>robusta</t> (intestinalis type A) embryo at Hotta Stage 25 (late tailbud III, ∼13 hours post-fertilization at 20°C), showing cell outlines and the oral siphon placode (OSP) rosette revealed by Phalloidin-AlexFluor546 staining. B ) In situ mRNA hybridization revealing Protocadherin.e ( Pcdh.e ) expression in the presumptive OSP, as well as in the Motor Ganglion Interneuron 2 (MGIN2) cells as previously reported . C ) Summary diagram of the separation of Six1/2+, future Protocadherin.e (Pcdh.e)- and Pitx- expressing oral siphon placode cells (red outline) from other Foxc+ cells (blue), mainly those contributing to the papillae. D ) Protein domain analysis diagram of Protocadherin.e (Pcdh.e) from SMART , showing presence of a signal peptide (red block), 6 extracellular cadherin repeats (CA) and a transmembrane (TM) domain, similar to the organization of vertebrate protocadherin-family proteins.
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A) <t>Ciona</t> <t>robusta</t> (intestinalis type A) embryo at Hotta Stage 25 (late tailbud III, ∼13 hours post-fertilization at 20°C), showing cell outlines and the oral siphon placode (OSP) rosette revealed by Phalloidin-AlexFluor546 staining. B ) In situ mRNA hybridization revealing Protocadherin.e ( Pcdh.e ) expression in the presumptive OSP, as well as in the Motor Ganglion Interneuron 2 (MGIN2) cells as previously reported . C ) Summary diagram of the separation of Six1/2+, future Protocadherin.e (Pcdh.e)- and Pitx- expressing oral siphon placode cells (red outline) from other Foxc+ cells (blue), mainly those contributing to the papillae. D ) Protein domain analysis diagram of Protocadherin.e (Pcdh.e) from SMART , showing presence of a signal peptide (red block), 6 extracellular cadherin repeats (CA) and a transmembrane (TM) domain, similar to the organization of vertebrate protocadherin-family proteins.
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A) <t>Ciona</t> <t>robusta</t> (intestinalis type A) embryo at Hotta Stage 25 (late tailbud III, ∼13 hours post-fertilization at 20°C), showing cell outlines and the oral siphon placode (OSP) rosette revealed by Phalloidin-AlexFluor546 staining. B ) In situ mRNA hybridization revealing Protocadherin.e ( Pcdh.e ) expression in the presumptive OSP, as well as in the Motor Ganglion Interneuron 2 (MGIN2) cells as previously reported . C ) Summary diagram of the separation of Six1/2+, future Protocadherin.e (Pcdh.e)- and Pitx- expressing oral siphon placode cells (red outline) from other Foxc+ cells (blue), mainly those contributing to the papillae. D ) Protein domain analysis diagram of Protocadherin.e (Pcdh.e) from SMART , showing presence of a signal peptide (red block), 6 extracellular cadherin repeats (CA) and a transmembrane (TM) domain, similar to the organization of vertebrate protocadherin-family proteins.
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A) <t>Ciona</t> <t>robusta</t> (intestinalis type A) embryo at Hotta Stage 25 (late tailbud III, ∼13 hours post-fertilization at 20°C), showing cell outlines and the oral siphon placode (OSP) rosette revealed by Phalloidin-AlexFluor546 staining. B ) In situ mRNA hybridization revealing Protocadherin.e ( Pcdh.e ) expression in the presumptive OSP, as well as in the Motor Ganglion Interneuron 2 (MGIN2) cells as previously reported . C ) Summary diagram of the separation of Six1/2+, future Protocadherin.e (Pcdh.e)- and Pitx- expressing oral siphon placode cells (red outline) from other Foxc+ cells (blue), mainly those contributing to the papillae. D ) Protein domain analysis diagram of Protocadherin.e (Pcdh.e) from SMART , showing presence of a signal peptide (red block), 6 extracellular cadherin repeats (CA) and a transmembrane (TM) domain, similar to the organization of vertebrate protocadherin-family proteins.
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A) <t>Ciona</t> <t>robusta</t> (intestinalis type A) embryo at Hotta Stage 25 (late tailbud III, ∼13 hours post-fertilization at 20°C), showing cell outlines and the oral siphon placode (OSP) rosette revealed by Phalloidin-AlexFluor546 staining. B ) In situ mRNA hybridization revealing Protocadherin.e ( Pcdh.e ) expression in the presumptive OSP, as well as in the Motor Ganglion Interneuron 2 (MGIN2) cells as previously reported . C ) Summary diagram of the separation of Six1/2+, future Protocadherin.e (Pcdh.e)- and Pitx- expressing oral siphon placode cells (red outline) from other Foxc+ cells (blue), mainly those contributing to the papillae. D ) Protein domain analysis diagram of Protocadherin.e (Pcdh.e) from SMART , showing presence of a signal peptide (red block), 6 extracellular cadherin repeats (CA) and a transmembrane (TM) domain, similar to the organization of vertebrate protocadherin-family proteins.
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A) <t>Ciona</t> <t>robusta</t> (intestinalis type A) embryo at Hotta Stage 25 (late tailbud III, ∼13 hours post-fertilization at 20°C), showing cell outlines and the oral siphon placode (OSP) rosette revealed by Phalloidin-AlexFluor546 staining. B ) In situ mRNA hybridization revealing Protocadherin.e ( Pcdh.e ) expression in the presumptive OSP, as well as in the Motor Ganglion Interneuron 2 (MGIN2) cells as previously reported . C ) Summary diagram of the separation of Six1/2+, future Protocadherin.e (Pcdh.e)- and Pitx- expressing oral siphon placode cells (red outline) from other Foxc+ cells (blue), mainly those contributing to the papillae. D ) Protein domain analysis diagram of Protocadherin.e (Pcdh.e) from SMART , showing presence of a signal peptide (red block), 6 extracellular cadherin repeats (CA) and a transmembrane (TM) domain, similar to the organization of vertebrate protocadherin-family proteins.
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A) <t>Ciona</t> <t>robusta</t> (intestinalis type A) embryo at Hotta Stage 25 (late tailbud III, ∼13 hours post-fertilization at 20°C), showing cell outlines and the oral siphon placode (OSP) rosette revealed by Phalloidin-AlexFluor546 staining. B ) In situ mRNA hybridization revealing Protocadherin.e ( Pcdh.e ) expression in the presumptive OSP, as well as in the Motor Ganglion Interneuron 2 (MGIN2) cells as previously reported . C ) Summary diagram of the separation of Six1/2+, future Protocadherin.e (Pcdh.e)- and Pitx- expressing oral siphon placode cells (red outline) from other Foxc+ cells (blue), mainly those contributing to the papillae. D ) Protein domain analysis diagram of Protocadherin.e (Pcdh.e) from SMART , showing presence of a signal peptide (red block), 6 extracellular cadherin repeats (CA) and a transmembrane (TM) domain, similar to the organization of vertebrate protocadherin-family proteins.
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A) Ciona robusta (intestinalis type A) embryo at Hotta Stage 25 (late tailbud III, ∼13 hours post-fertilization at 20°C), showing cell outlines and the oral siphon placode (OSP) rosette revealed by Phalloidin-AlexFluor546 staining. B ) In situ mRNA hybridization revealing Protocadherin.e ( Pcdh.e ) expression in the presumptive OSP, as well as in the Motor Ganglion Interneuron 2 (MGIN2) cells as previously reported . C ) Summary diagram of the separation of Six1/2+, future Protocadherin.e (Pcdh.e)- and Pitx- expressing oral siphon placode cells (red outline) from other Foxc+ cells (blue), mainly those contributing to the papillae. D ) Protein domain analysis diagram of Protocadherin.e (Pcdh.e) from SMART , showing presence of a signal peptide (red block), 6 extracellular cadherin repeats (CA) and a transmembrane (TM) domain, similar to the organization of vertebrate protocadherin-family proteins.

Journal: bioRxiv

Article Title: A protocadherin mediates cell-cell adhesion and integrity of the oral placode in the tunicate Ciona

doi: 10.1101/2025.07.11.664433

Figure Lengend Snippet: A) Ciona robusta (intestinalis type A) embryo at Hotta Stage 25 (late tailbud III, ∼13 hours post-fertilization at 20°C), showing cell outlines and the oral siphon placode (OSP) rosette revealed by Phalloidin-AlexFluor546 staining. B ) In situ mRNA hybridization revealing Protocadherin.e ( Pcdh.e ) expression in the presumptive OSP, as well as in the Motor Ganglion Interneuron 2 (MGIN2) cells as previously reported . C ) Summary diagram of the separation of Six1/2+, future Protocadherin.e (Pcdh.e)- and Pitx- expressing oral siphon placode cells (red outline) from other Foxc+ cells (blue), mainly those contributing to the papillae. D ) Protein domain analysis diagram of Protocadherin.e (Pcdh.e) from SMART , showing presence of a signal peptide (red block), 6 extracellular cadherin repeats (CA) and a transmembrane (TM) domain, similar to the organization of vertebrate protocadherin-family proteins.

Article Snippet: Adult Ciona robusta specimens were collected in California, around San Diego (M-REP) or Los Angeles/Orange County (Marinus Scientific).

Techniques: Staining, In Situ, Hybridization, Expressing, Blocking Assay