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- Publisher Website: 10.1007/s00425-004-1306-6
- Scopus: eid_2-s2.0-7044234943
- PMID: 15197596
- WOS: WOS:000224614600010
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Article: Expression of proteinase inhibitor II proteins during floral development in Solanum americanum
Title | Expression of proteinase inhibitor II proteins during floral development in Solanum americanum |
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Authors | |
Keywords | Nightshade Ovule Programmed cell death Proteolysis Style TUNEL analysis |
Issue Date | 2004 |
Publisher | Springer Verlag. The Journal's web site is located at http://link.springer.de/link/service/journals/00425 |
Citation | Planta, 2004, v. 219 n. 6, p. 1010-1022 How to Cite? |
Abstract | The heterologous expression of serine proteinase inhibitor II (PIN2) proteins confers insect resistance in transgenic plants, but little is known of their endogenous roles. We have cloned two cDNAs encoding Solanum americanum PIN2 proteins, SaPIN2a and SaPIN2b. SaPIN2a is highly expressed in stem, particularly in the phloem, suggesting it could possibly regulate proteolysis in the sieve elements. When SaPIN2a was expressed in transgenic lettuce, we observed an inhibition of endogenous trypsin- and chymotrypsin-like activities. Here, we demonstrate that both SaPIN2a and SaPIN2b are expressed in floral tissues that are destined to undergo developmental programmed cell death (PCD), suggesting possible endogenous roles in inhibiting trypsin- and chymotrypsin-like activities during flower development. Northern and western blot analyses revealed that SaPIN2a and SaPIN2b mRNAs and proteins show highest expression early in floral development. In situ hybridization analysis and immunolocalization on floral sections, localized SaPIN2a and SaPIN2b mRNAs and their proteins to tissues that would apparently undergo PCD: the ovules, the stylar transmitting tissue, the stigma and the vascular bundles. Detection of PCD in floral sections was achieved using terminal deoxynucleotidyltransferase- mediated dUTP nick end labeling (TUNEL) analysis. Examination of the mid-style before, and 1 day after, pollination revealed that high expression of SaPIN2a and SaPIN2b in the style was inversely correlated with PCD. © Springer-Verlag 2004. |
Persistent Identifier | http://hdl.handle.net/10722/179164 |
ISSN | 2023 Impact Factor: 3.6 2023 SCImago Journal Rankings: 0.944 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Sin, SF | en_US |
dc.contributor.author | Chye, ML | en_US |
dc.date.accessioned | 2012-12-19T09:52:28Z | - |
dc.date.available | 2012-12-19T09:52:28Z | - |
dc.date.issued | 2004 | en_US |
dc.identifier.citation | Planta, 2004, v. 219 n. 6, p. 1010-1022 | en_US |
dc.identifier.issn | 0032-0935 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/179164 | - |
dc.description.abstract | The heterologous expression of serine proteinase inhibitor II (PIN2) proteins confers insect resistance in transgenic plants, but little is known of their endogenous roles. We have cloned two cDNAs encoding Solanum americanum PIN2 proteins, SaPIN2a and SaPIN2b. SaPIN2a is highly expressed in stem, particularly in the phloem, suggesting it could possibly regulate proteolysis in the sieve elements. When SaPIN2a was expressed in transgenic lettuce, we observed an inhibition of endogenous trypsin- and chymotrypsin-like activities. Here, we demonstrate that both SaPIN2a and SaPIN2b are expressed in floral tissues that are destined to undergo developmental programmed cell death (PCD), suggesting possible endogenous roles in inhibiting trypsin- and chymotrypsin-like activities during flower development. Northern and western blot analyses revealed that SaPIN2a and SaPIN2b mRNAs and proteins show highest expression early in floral development. In situ hybridization analysis and immunolocalization on floral sections, localized SaPIN2a and SaPIN2b mRNAs and their proteins to tissues that would apparently undergo PCD: the ovules, the stylar transmitting tissue, the stigma and the vascular bundles. Detection of PCD in floral sections was achieved using terminal deoxynucleotidyltransferase- mediated dUTP nick end labeling (TUNEL) analysis. Examination of the mid-style before, and 1 day after, pollination revealed that high expression of SaPIN2a and SaPIN2b in the style was inversely correlated with PCD. © Springer-Verlag 2004. | en_US |
dc.language | eng | en_US |
dc.publisher | Springer Verlag. The Journal's web site is located at http://link.springer.de/link/service/journals/00425 | en_US |
dc.relation.ispartof | Planta | en_US |
dc.subject | Nightshade | - |
dc.subject | Ovule | - |
dc.subject | Programmed cell death | - |
dc.subject | Proteolysis | - |
dc.subject | Style | - |
dc.subject | TUNEL analysis | - |
dc.subject.mesh | Apoptosis - Physiology | en_US |
dc.subject.mesh | Flowers - Growth & Development - Metabolism | en_US |
dc.subject.mesh | Plant Proteins - Biosynthesis - Physiology | en_US |
dc.subject.mesh | Rna, Messenger - Metabolism | en_US |
dc.subject.mesh | Rna, Plant - Metabolism | en_US |
dc.subject.mesh | Solanum - Growth & Development - Metabolism | en_US |
dc.subject.mesh | Tissue Distribution | en_US |
dc.title | Expression of proteinase inhibitor II proteins during floral development in Solanum americanum | en_US |
dc.type | Article | en_US |
dc.identifier.email | Chye, ML: mlchye@hkucc.hku.hk | en_US |
dc.identifier.authority | Chye, ML=rp00687 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1007/s00425-004-1306-6 | en_US |
dc.identifier.pmid | 15197596 | - |
dc.identifier.scopus | eid_2-s2.0-7044234943 | en_US |
dc.identifier.hkuros | 96631 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-7044234943&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 219 | en_US |
dc.identifier.issue | 6 | en_US |
dc.identifier.spage | 1010 | en_US |
dc.identifier.epage | 1022 | en_US |
dc.identifier.isi | WOS:000224614600010 | - |
dc.publisher.place | Germany | en_US |
dc.identifier.scopusauthorid | Sin, SF=7006553279 | en_US |
dc.identifier.scopusauthorid | Chye, ML=7003905460 | en_US |
dc.identifier.issnl | 0032-0935 | - |