http://www.cnr.it/ontology/cnr/individuo/prodotto/ID11499
Streptococcus pneumoniae DivIVA: localization and interactions in a MinCD-free context. (Articolo in rivista)
- Type
- Label
- Streptococcus pneumoniae DivIVA: localization and interactions in a MinCD-free context. (Articolo in rivista) (literal)
- Anno
- 2007-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1128/JB.01168-06 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Fadda D; Santona A; D'Ulisse V; Ghelardini P; Ennas MG; Whalen MB; Massidda O. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Dipartimento di Scienze e Tecnologie Biomediche, Sez. Microbiologia Medica, Universita` di Cagliari,
Dipartimento di Biologia, Universita` \"Tor Vergata,\"
Istituto di Biologia e Patologia Molecolare CNR
Dipartimento di Citomorfologia, Universita` di Cagliari
Dipartimento di Bioinformatica, SharDna Life Sciences,
09100 Pula, Cagliari, Italy5 (literal)
- Titolo
- Streptococcus pneumoniae DivIVA: localization and interactions in a MinCD-free context. (literal)
- Abstract
- To clarify the function of DivIVA in Streptococcus pneumoniae, we localized this protein in exponentially
growing cells by both immunofluorescence microscopy and immunoelectron microscopy and found that S.
pneumoniae DivIVA (DivIVASPN) had a unique localization profile: it was present simultaneously both as a ring
at the division septum and as dots at the cell poles. Double-immunofluorescence analysis suggested that
DivIVA is recruited to the septum at a later stage than FtsZ and is retained at the poles after cell separation.
All the other cell division proteins that we tested were localized in the divIVA null mutant, although the
percentage of cells having constricted Z rings was significantly reduced. In agreement with its localization
profile and consistent with its coiled-coil nature, DivIVA interacted with itself and with a number of known or
putative S. pneumoniae cell division proteins. Finally, a missense divIVA mutant, obtained by allelic replacement,
allowed us to correlate, at the molecular level, the specific interactions and some of the facets of the
divIVA mutant phenotype. Taken together, the results suggest that although the possibility of a direct role in
chromosome segregation cannot be ruled out, DivIVA in S. pneumoniae seems to be primarily involved in the
formation and maturation of the cell poles. The localization and the interaction properties of DivIVASPN raise
the intriguing possibility that a common, MinCD-independent function evolved differently in the various host
backgrounds. (literal)
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- Autore CNR
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