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exhibits. TPX2 α5-7 is unique from the remainder of the protein in that it has conserved
areas in its amino acid sequence that share sequence similarity with two recognized γ-TuRC nucleation activator motifs: SPM and γ-TuRC.
However, in vitro ubiquitination assays have proven that only the
1st 83 amino acids of the N-terminal area of TPX2 together with the KEN box are pertinent for
recognition by Cdh1, an activator of the APC/C.
The instability and fall in TPX2 at mitotic exit is dependent on both the anaphase-endorsing advanced/cyclosome (APC/C) and an ubiquitin ligase integral in mitotic development, alongside with APC/C's activator protein, Cdh1.
Moreover, the Cdh1-TPX2 binding conversation makes the TPX2 stability witnessed
for the duration of mitosis up right until mitotic exit: The amino-terminal region of Cdh1 (amino acids
1-125) can act as a dominant adverse mutant when expressed
in mammalian cells, stabilizing APC/CCdh1 substrates these as TPX2
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the C-terminal residues that interact with Eg5 are important
for microtubule branching nucleation as effectively.
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