Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2002-3-21
pubmed:abstractText
The subpellicular microtubules of the trypanosome cytoskeleton are cross-linked to each other and the plasma membrane, creating a cage-like structure. We have isolated, from Trypanosoma brucei, two related low-molecular-weight cytoskeleton-associated proteins (15- and 17-kDa), called CAP15 and CAP17, which are differentially expressed during the life cycle. Immunolabeling shows a corset-like colocalization of both CAPs and tubulin. Western blot and electron microscope analyses show CAP15 and CAP17 labeling on detergent-extracted cytoskeletons. However, the localization of both proteins is restricted to the anterior, microtubule minus, and less dynamic half of the corset. CAP15 and CAP17 share properties of microtubule-associated proteins when expressed in heterologous cells (Chinese hamster ovary and HeLa), colocalization with their microtubules, induction of microtubule bundle formation, cold resistance, and insensitivity to nocodazole. When overexpressed in T. brucei, both CAP15 and CAP17 cover the whole subpellicular corset and induce morphological disorders, cell cycle-based abnormalities, and subsequent asymmetric cytokinesis.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-10574712, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-1348252, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-1478963, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-1524213, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-1559265, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-1614728, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-1876188, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-2034124, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-2190996, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-2302174, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-2568647, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-2582498, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-2649249, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-2883007, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-3360790, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-3393912, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-6144043, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-7442712, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-7622564, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-7673343, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-7706399, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-7724233, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-7755992, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-7896879, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-7954847, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-7986649, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-8459837, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-8700896, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-8801031, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-9127738, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-9600916, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-9653123, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-9662023, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-9747975, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-9757832, http://linkedlifedata.com/resource/pubmed/commentcorrection/11907282-9915583
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1059-1524
pubmed:author
pubmed:issnType
Print
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1058-70
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:11907282-Amino Acid Sequence, pubmed-meshheading:11907282-Animals, pubmed-meshheading:11907282-Antimalarials, pubmed-meshheading:11907282-CHO Cells, pubmed-meshheading:11907282-Cricetinae, pubmed-meshheading:11907282-Cytoskeleton, pubmed-meshheading:11907282-Doxycycline, pubmed-meshheading:11907282-Flagella, pubmed-meshheading:11907282-HeLa Cells, pubmed-meshheading:11907282-Humans, pubmed-meshheading:11907282-Microscopy, Electron, pubmed-meshheading:11907282-Microtubule-Associated Proteins, pubmed-meshheading:11907282-Microtubules, pubmed-meshheading:11907282-Molecular Sequence Data, pubmed-meshheading:11907282-Protozoan Proteins, pubmed-meshheading:11907282-Recombinant Proteins, pubmed-meshheading:11907282-Sequence Alignment, pubmed-meshheading:11907282-Trypanosoma brucei brucei
pubmed:year
2002
pubmed:articleTitle
Two related subpellicular cytoskeleton-associated proteins in Trypanosoma brucei stabilize microtubules.
pubmed:affiliation
Laboratoire de Parasitologie Moléculaire, Université Victor Segalen de Bordeaux II, Unité Mixte Recherche-5016 Centre National de la Recherche Scientifique, 33076 Bordeaux, France.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't