Cultural advice

The Australian National University acknowledges, celebrates and pays our respects to the Ngunnawal and Ngambri people of the Canberra region and to all First Nations Australians on whose traditional lands we meet and work, and whose cultures are among the oldest continuing cultures in human history.

Aboriginal and Torres Strait Islander peoples are advised that ANU Library collections may include images, names, voices, and other representations of deceased persons.

Material in the collection may contain terms, language or views that reflect the period in which the item was created and may be considered inappropriate today.

Molecular Cloning and Characterization of Fox Testis Kinectin

dc.contributor.authorXu, J
dc.contributor.authorBird, Phillip I
dc.contributor.authorBradley, Mark P
dc.contributor.authorJanssens, Peter
dc.contributor.authorHardy, Christopher C
dc.date.accessioned2015-12-13T23:24:32Z
dc.date.available2015-12-13T23:24:32Z
dc.date.issued2002
dc.date.updated2015-12-12T09:20:52Z
dc.description.abstractKinectin was isolated and characterized from a fox testis cDNA library using a monoclonal antibody (FTA-1) raised against testis surface proteins. The cDNA sequence of 4,479 nucleotides encodes an ORF of 1,330 amino acids (aa) with high homology to mouse, human, and chicken kinectins (GenBank Accession Number AF095786). Southern analysis was used to show that genes homologous to kinectin are present in several mammal species and in at least one marsupial, but not in bacteria. Alternatively spliced forms of fox kinectin were identified, and one of these is uniquely expressed in brain and spleen tissues. Kinectin expression was highest in testis relative to other tissues examined. Sequence analysis and comparisons between species revealed that kinectin encodes multiple α-helical coiled coils predicted to form dimers, and is, therefore, likely to exist as a dimer. The results presented in this article suggest that kinectin is required for spermatogenesis, but is not a likely candidate for use in immunocontraceptive vaccines.
dc.identifier.issn1040-452X
dc.identifier.urihttp://hdl.handle.net/1885/92264
dc.publisherJohn Wiley & Sons Inc
dc.sourceMolecular Reproduction and Development
dc.subjectKeywords: complementary DNA; kinetin; monoclonal antibody; animal tissue; article; bacterium; brain tissue; chicken; DNA library; DNA sequence; fox; human; marsupial; molecular cloning; mouse; nonhuman; nucleotide sequence; priority journal; sequence homology; Sout Differential splicing; Motor protein; Spermatogenesis
dc.titleMolecular Cloning and Characterization of Fox Testis Kinectin
dc.typeJournal article
local.bibliographicCitation.issue1
local.bibliographicCitation.lastpage46
local.bibliographicCitation.startpage37
local.contributor.affiliationXu, J, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationBird, Phillip I, Monash University
local.contributor.affiliationBradley, Mark P, CRC for the Biological Control of Pest Animals (CSIRO)
local.contributor.affiliationJanssens, Peter, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationHardy, Christopher C, CRC for the Biological Control of Pest Animals (CSIRO)
local.contributor.authoruidXu, J, u900644
local.contributor.authoruidJanssens, Peter, u6700633
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor060106 - Cellular Interactions (incl. Adhesion, Matrix, Cell Wall)
local.identifier.ariespublicationMigratedxPub23297
local.identifier.citationvolume62
local.identifier.doi10.1002/mrd.10066
local.identifier.scopusID2-s2.0-0036203163
local.type.statusPublished Version

Downloads