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TPPP/p25 Promotes Tubulin Assemblies and Blocks Mitotic Spindle Formation

Recently, we isolated from bovine brain a protein, TPPP/p25 and identified as p25, a brain-specific protein that induced aberrant tubulin assemblies. The primary sequence of this protein differs from that of other proteins identified so far; however, it shows high homology with p25-like hypothetical...

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Bibliographic Details
Published in:Proceedings of the National Academy of Sciences - PNAS 2003-11, Vol.100 (24), p.13976-13981
Main Authors: Tirián, L., Hlavanda, E., Oláh, J., Horváth, I., Orosz, F., Szabó, B., Kovács, J., Szabad, J., Ovádi, J.
Format: Article
Language:English
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Summary:Recently, we isolated from bovine brain a protein, TPPP/p25 and identified as p25, a brain-specific protein that induced aberrant tubulin assemblies. The primary sequence of this protein differs from that of other proteins identified so far; however, it shows high homology with p25-like hypothetical proteins sought via Blast. Here, we characterized the binding of TPPP/p25 to tubulin by means of surface plasmon resonance; the kinetic parameters are as follows:$k_{on},\>2.4 \times 10^4\>M^{-1}\!\cdot\!s^{-1};\>k_{off},\>5.4 \times 10^{-3}\>s^{-1}$; and$K_d,\>2.3 \times 10^{-7}\>M$. This protein at substoichometric concentration promotes the polymerization of tubulin into double-walled tubules and polymorphic aggregates or bundles paclitaxel-stabilized microtubules as judged by quantitative data of electron and atomic force microscopies. Injection of bovine TPPP/p25 into cleavage Drosophila embryos expressing tubulin-GFP fusion protein reveals that TPPP/p25 inhibits mitotic spindle assembly and nuclear envelope breakdown without affecting other cellular events like centrosome replication and separation, microtubule nucleation by the centrosomes, and nuclear growth. GTP counteracts TPPP/p25 both in vitro and in vivo.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.2436331100