| Literature DB >> 10188731 |
J P Juwana1, P Henderikx, A Mischo, A Wadle, N Fadle, K Gerlach, J W Arends, H Hoogenboom, M Pfreundschuh, C Renner.
Abstract
Mutations in the adenomatous polyposis coli (APC) gene are linked to the dysplastic transformation of colorectal polyps and represent an early step in the development of colorectal tumors. Ninety-four percent of all mutations result in the expression of a truncated APC protein lacking the C-terminal region. The C-terminal region of the APC protein may have a tumor suppressor function as its absence appears to be linked to the development of dysplastic lesions. Recently, we discovered and characterized a protein called RP1 which binds specifically to the C-terminal region of the APC protein. We show now that RP1 and the other known members of the EB/RP family (EB1 and RP3) also bind directly to tubulin, both in vitro and in vivo. Immunohistochemical analyses reveal a distinct staining pattern during interphase as well as an association of RP1/EB1 with mitotic microtubule structures. The previously described puncta of the APC protein at the leading edge of membrane protrusions contact microtubule fibers that contain RP1 or EB1.Entities:
Mesh:
Substances:
Year: 1999 PMID: 10188731 DOI: 10.1002/(sici)1097-0215(19990412)81:2<275::aid-ijc18>3.0.co;2-z
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396