Thrittene, homologous with somatostatin-28(1-13), is a novel peptide in mammalian gut and circulation

Autores
Ensinck, John W.; Baskin, Denis G.; Vahl, Torsten P.; Vogel, Robin E.; Laschansky, Ellen C.; Francis, Bruce H.; Hoffman, Ross C.; Krakover, Jonathan D.; Stamm, Michael R.; Low, Malcolm J.; Rubinstein, Marcelo; Otero Corchon, Veronica; D'Alessio, David A.
Año de publicación
2002
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Preprosomatostatin is a gene expressed ubiquitously among vertebrates, and at least two duplications of this gene have occurred during evolution. Somatostatin-28 (S-28) and somatostatin-14 (S-14), C-terminal products of prosomatostatin (ProS), are differentially expressed in mammalian neurons, D cells, and enterocytes. One pathway for the generation of S-14 entails the excision of Arg13-Lys14 in S-28, leading to equivalent amounts of S-28(1-12). Using an antiserum (F-4), directed to the N-terminal region of S-28 that does not react with S-28(1-12), we detected a peptide, in addition to S-28 and ProS, that was present in human plasma and in the intestinal tract of rats and monkeys. This F-4 reacting peptide was purified from monkey ileum; and its amino acid sequence, molecular mass, and chromatographic characteristics conformed to those of S-28(1-13), a peptide not described heretofore. When extracts of the small intestine were measured by RIA, there was a discordance in the ratio of peptides reacting with F-4 and those containing the C terminus of ProS, suggesting sites of synthesis for S-28(1-13) distinct from those for S-14 and S-28. This was supported by immunocytochemistry, wherein F-4 reactivity was localized in gastrointestinal (GI) endocrine cells and a widespread plexus of neurons within the wall of the distal gut while immunoreactivity to C-terminal domains of S-14 and S-28 in these neurons was absent. Further, F-4 immunoreactivity persisted in similar GI endocrine cells and myenteric neurons in mice with a targeted deletion of the preprosomatostatin gene. We believe that these data suggest a novel peptide produced in the mammalian gut, homologous with the 13 residues of the proximal region of S-28 but not derived from the Pros gene. Pending characterization of the gene from which this peptide is derived, its distribution, and function, we have designated this peptide as thrittene. Its localization in both GI endocrine cells and gut neurons suggests that thrittene may function as both a hormone and neurotransmitter.
Fil: Ensinck, John W.. University of Washington; Estados Unidos
Fil: Baskin, Denis G.. University of Washington; Estados Unidos. Department of Veterans Affairs Puget Sound Health Care System; Estados Unidos
Fil: Vahl, Torsten P.. University of Cincinnati; Estados Unidos
Fil: Vogel, Robin E.. University of Washington; Estados Unidos
Fil: Laschansky, Ellen C.. University of Washington; Estados Unidos
Fil: Francis, Bruce H.. University of Washington; Estados Unidos
Fil: Hoffman, Ross C.. ZymoGenetics; Estados Unidos
Fil: Krakover, Jonathan D.. ZymoGenetics; Estados Unidos
Fil: Stamm, Michael R.. ZymoGenetics; Estados Unidos
Fil: Low, Malcolm J.. Oregon Health Sciences University; Estados Unidos
Fil: Rubinstein, Marcelo. Oregon Health Sciences University; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Otero Corchon, Veronica. Oregon Health Sciences University; Estados Unidos
Fil: D'Alessio, David A.. University of Cincinnati; Estados Unidos
Materia
Somatostatina
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/79827

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network_name_str CONICET Digital (CONICET)
spelling Thrittene, homologous with somatostatin-28(1-13), is a novel peptide in mammalian gut and circulationEnsinck, John W.Baskin, Denis G.Vahl, Torsten P.Vogel, Robin E.Laschansky, Ellen C.Francis, Bruce H.Hoffman, Ross C.Krakover, Jonathan D.Stamm, Michael R.Low, Malcolm J.Rubinstein, MarceloOtero Corchon, VeronicaD'Alessio, David A.Somatostatinahttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3Preprosomatostatin is a gene expressed ubiquitously among vertebrates, and at least two duplications of this gene have occurred during evolution. Somatostatin-28 (S-28) and somatostatin-14 (S-14), C-terminal products of prosomatostatin (ProS), are differentially expressed in mammalian neurons, D cells, and enterocytes. One pathway for the generation of S-14 entails the excision of Arg13-Lys14 in S-28, leading to equivalent amounts of S-28(1-12). Using an antiserum (F-4), directed to the N-terminal region of S-28 that does not react with S-28(1-12), we detected a peptide, in addition to S-28 and ProS, that was present in human plasma and in the intestinal tract of rats and monkeys. This F-4 reacting peptide was purified from monkey ileum; and its amino acid sequence, molecular mass, and chromatographic characteristics conformed to those of S-28(1-13), a peptide not described heretofore. When extracts of the small intestine were measured by RIA, there was a discordance in the ratio of peptides reacting with F-4 and those containing the C terminus of ProS, suggesting sites of synthesis for S-28(1-13) distinct from those for S-14 and S-28. This was supported by immunocytochemistry, wherein F-4 reactivity was localized in gastrointestinal (GI) endocrine cells and a widespread plexus of neurons within the wall of the distal gut while immunoreactivity to C-terminal domains of S-14 and S-28 in these neurons was absent. Further, F-4 immunoreactivity persisted in similar GI endocrine cells and myenteric neurons in mice with a targeted deletion of the preprosomatostatin gene. We believe that these data suggest a novel peptide produced in the mammalian gut, homologous with the 13 residues of the proximal region of S-28 but not derived from the Pros gene. Pending characterization of the gene from which this peptide is derived, its distribution, and function, we have designated this peptide as thrittene. Its localization in both GI endocrine cells and gut neurons suggests that thrittene may function as both a hormone and neurotransmitter.Fil: Ensinck, John W.. University of Washington; Estados UnidosFil: Baskin, Denis G.. University of Washington; Estados Unidos. Department of Veterans Affairs Puget Sound Health Care System; Estados UnidosFil: Vahl, Torsten P.. University of Cincinnati; Estados UnidosFil: Vogel, Robin E.. University of Washington; Estados UnidosFil: Laschansky, Ellen C.. University of Washington; Estados UnidosFil: Francis, Bruce H.. University of Washington; Estados UnidosFil: Hoffman, Ross C.. ZymoGenetics; Estados UnidosFil: Krakover, Jonathan D.. ZymoGenetics; Estados UnidosFil: Stamm, Michael R.. ZymoGenetics; Estados UnidosFil: Low, Malcolm J.. Oregon Health Sciences University; Estados UnidosFil: Rubinstein, Marcelo. Oregon Health Sciences University; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Otero Corchon, Veronica. Oregon Health Sciences University; Estados UnidosFil: D'Alessio, David A.. University of Cincinnati; Estados UnidosOxford University Press2002-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/79827Ensinck, John W.; Baskin, Denis G.; Vahl, Torsten P.; Vogel, Robin E.; Laschansky, Ellen C.; et al.; Thrittene, homologous with somatostatin-28(1-13), is a novel peptide in mammalian gut and circulation; Oxford University Press; Endocrinology; 143; 7; 7-2002; 2599-26090013-7227CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1210/endo.143.7.8904info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pubmed/12072392info:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/endo/article/143/7/2599/2989507info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:04:29Zoai:ri.conicet.gov.ar:11336/79827instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:04:29.508CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Thrittene, homologous with somatostatin-28(1-13), is a novel peptide in mammalian gut and circulation
title Thrittene, homologous with somatostatin-28(1-13), is a novel peptide in mammalian gut and circulation
spellingShingle Thrittene, homologous with somatostatin-28(1-13), is a novel peptide in mammalian gut and circulation
Ensinck, John W.
Somatostatina
title_short Thrittene, homologous with somatostatin-28(1-13), is a novel peptide in mammalian gut and circulation
title_full Thrittene, homologous with somatostatin-28(1-13), is a novel peptide in mammalian gut and circulation
title_fullStr Thrittene, homologous with somatostatin-28(1-13), is a novel peptide in mammalian gut and circulation
title_full_unstemmed Thrittene, homologous with somatostatin-28(1-13), is a novel peptide in mammalian gut and circulation
title_sort Thrittene, homologous with somatostatin-28(1-13), is a novel peptide in mammalian gut and circulation
dc.creator.none.fl_str_mv Ensinck, John W.
Baskin, Denis G.
Vahl, Torsten P.
Vogel, Robin E.
Laschansky, Ellen C.
Francis, Bruce H.
Hoffman, Ross C.
Krakover, Jonathan D.
Stamm, Michael R.
Low, Malcolm J.
Rubinstein, Marcelo
Otero Corchon, Veronica
D'Alessio, David A.
author Ensinck, John W.
author_facet Ensinck, John W.
Baskin, Denis G.
Vahl, Torsten P.
Vogel, Robin E.
Laschansky, Ellen C.
Francis, Bruce H.
Hoffman, Ross C.
Krakover, Jonathan D.
Stamm, Michael R.
Low, Malcolm J.
Rubinstein, Marcelo
Otero Corchon, Veronica
D'Alessio, David A.
author_role author
author2 Baskin, Denis G.
Vahl, Torsten P.
Vogel, Robin E.
Laschansky, Ellen C.
Francis, Bruce H.
Hoffman, Ross C.
Krakover, Jonathan D.
Stamm, Michael R.
Low, Malcolm J.
Rubinstein, Marcelo
Otero Corchon, Veronica
D'Alessio, David A.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Somatostatina
topic Somatostatina
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.1
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv Preprosomatostatin is a gene expressed ubiquitously among vertebrates, and at least two duplications of this gene have occurred during evolution. Somatostatin-28 (S-28) and somatostatin-14 (S-14), C-terminal products of prosomatostatin (ProS), are differentially expressed in mammalian neurons, D cells, and enterocytes. One pathway for the generation of S-14 entails the excision of Arg13-Lys14 in S-28, leading to equivalent amounts of S-28(1-12). Using an antiserum (F-4), directed to the N-terminal region of S-28 that does not react with S-28(1-12), we detected a peptide, in addition to S-28 and ProS, that was present in human plasma and in the intestinal tract of rats and monkeys. This F-4 reacting peptide was purified from monkey ileum; and its amino acid sequence, molecular mass, and chromatographic characteristics conformed to those of S-28(1-13), a peptide not described heretofore. When extracts of the small intestine were measured by RIA, there was a discordance in the ratio of peptides reacting with F-4 and those containing the C terminus of ProS, suggesting sites of synthesis for S-28(1-13) distinct from those for S-14 and S-28. This was supported by immunocytochemistry, wherein F-4 reactivity was localized in gastrointestinal (GI) endocrine cells and a widespread plexus of neurons within the wall of the distal gut while immunoreactivity to C-terminal domains of S-14 and S-28 in these neurons was absent. Further, F-4 immunoreactivity persisted in similar GI endocrine cells and myenteric neurons in mice with a targeted deletion of the preprosomatostatin gene. We believe that these data suggest a novel peptide produced in the mammalian gut, homologous with the 13 residues of the proximal region of S-28 but not derived from the Pros gene. Pending characterization of the gene from which this peptide is derived, its distribution, and function, we have designated this peptide as thrittene. Its localization in both GI endocrine cells and gut neurons suggests that thrittene may function as both a hormone and neurotransmitter.
Fil: Ensinck, John W.. University of Washington; Estados Unidos
Fil: Baskin, Denis G.. University of Washington; Estados Unidos. Department of Veterans Affairs Puget Sound Health Care System; Estados Unidos
Fil: Vahl, Torsten P.. University of Cincinnati; Estados Unidos
Fil: Vogel, Robin E.. University of Washington; Estados Unidos
Fil: Laschansky, Ellen C.. University of Washington; Estados Unidos
Fil: Francis, Bruce H.. University of Washington; Estados Unidos
Fil: Hoffman, Ross C.. ZymoGenetics; Estados Unidos
Fil: Krakover, Jonathan D.. ZymoGenetics; Estados Unidos
Fil: Stamm, Michael R.. ZymoGenetics; Estados Unidos
Fil: Low, Malcolm J.. Oregon Health Sciences University; Estados Unidos
Fil: Rubinstein, Marcelo. Oregon Health Sciences University; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Otero Corchon, Veronica. Oregon Health Sciences University; Estados Unidos
Fil: D'Alessio, David A.. University of Cincinnati; Estados Unidos
description Preprosomatostatin is a gene expressed ubiquitously among vertebrates, and at least two duplications of this gene have occurred during evolution. Somatostatin-28 (S-28) and somatostatin-14 (S-14), C-terminal products of prosomatostatin (ProS), are differentially expressed in mammalian neurons, D cells, and enterocytes. One pathway for the generation of S-14 entails the excision of Arg13-Lys14 in S-28, leading to equivalent amounts of S-28(1-12). Using an antiserum (F-4), directed to the N-terminal region of S-28 that does not react with S-28(1-12), we detected a peptide, in addition to S-28 and ProS, that was present in human plasma and in the intestinal tract of rats and monkeys. This F-4 reacting peptide was purified from monkey ileum; and its amino acid sequence, molecular mass, and chromatographic characteristics conformed to those of S-28(1-13), a peptide not described heretofore. When extracts of the small intestine were measured by RIA, there was a discordance in the ratio of peptides reacting with F-4 and those containing the C terminus of ProS, suggesting sites of synthesis for S-28(1-13) distinct from those for S-14 and S-28. This was supported by immunocytochemistry, wherein F-4 reactivity was localized in gastrointestinal (GI) endocrine cells and a widespread plexus of neurons within the wall of the distal gut while immunoreactivity to C-terminal domains of S-14 and S-28 in these neurons was absent. Further, F-4 immunoreactivity persisted in similar GI endocrine cells and myenteric neurons in mice with a targeted deletion of the preprosomatostatin gene. We believe that these data suggest a novel peptide produced in the mammalian gut, homologous with the 13 residues of the proximal region of S-28 but not derived from the Pros gene. Pending characterization of the gene from which this peptide is derived, its distribution, and function, we have designated this peptide as thrittene. Its localization in both GI endocrine cells and gut neurons suggests that thrittene may function as both a hormone and neurotransmitter.
publishDate 2002
dc.date.none.fl_str_mv 2002-07
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/79827
Ensinck, John W.; Baskin, Denis G.; Vahl, Torsten P.; Vogel, Robin E.; Laschansky, Ellen C.; et al.; Thrittene, homologous with somatostatin-28(1-13), is a novel peptide in mammalian gut and circulation; Oxford University Press; Endocrinology; 143; 7; 7-2002; 2599-2609
0013-7227
CONICET Digital
CONICET
url http://hdl.handle.net/11336/79827
identifier_str_mv Ensinck, John W.; Baskin, Denis G.; Vahl, Torsten P.; Vogel, Robin E.; Laschansky, Ellen C.; et al.; Thrittene, homologous with somatostatin-28(1-13), is a novel peptide in mammalian gut and circulation; Oxford University Press; Endocrinology; 143; 7; 7-2002; 2599-2609
0013-7227
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1210/endo.143.7.8904
info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pubmed/12072392
info:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/endo/article/143/7/2599/2989507
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Oxford University Press
publisher.none.fl_str_mv Oxford University Press
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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