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Mitotic spindle checkpoint component Mad2 Identifiers Organism S. cerevisiae S288c Symbol Mad2 Alt. symbols YJL030W Entrez 853422 RefSeq (mRNA) NM_001181464 RefSeq (Prot) NP_012504 UniProt P40958 Other data Chromosome X: 0.39 - 0.39 Mb Mad2 (mitotic arrest deficient 2) is an essential spindle checkpoint protein. The spindle checkpoint system is a regulatory system that restrains progression through the metaphase-to-anaphase transition. The Mad2 gene was first identified in the yeast S. cerevisiae in a screen for genes which when mutated would confer sensitivity to microtubule poisons.[1] The human orthologues of Mad2 (MAD2L1 and MAD2L2) were first cloned in a search for human cDNAs that would rescue the microtubule poison-sensitivity of a yeast strain in which a kinetochore binding protein was missing.[2] The protein was shown to be present at unattached kinetochores and antibody inhibition studies demonstrated it was essential to execute a block in the metaphase-to-anaphase transition in response to the microtubule poison nocodazole.[2] Subsequent cloning of the Xenopus laevis orthologue, facilitated by the sharing of the human sequence, allowed for the characterization of the mitotic checkpoint in egg extracts.[3] Contents 1 Metaphase-to-anaphase transition 2 Mad2 conformers 3 Mad2 activation in the spindle assembly checkpoint 4 Future work 5 References Metaphase-to-anaphase transition[edit] In response to kinetochores that are not bi-oriented, the checkpoint is turned on. APC/Cdc20 remains inactive preventing securin destruction and separase activation.[4] Progression from metaphase to anaphase is marked by sister chromatid separation. The cell cycle surveillance mechanism that prevents sister-chromatid separation and transition into anaphase is called the spindle checkpoint. As a safeguard against chromosome segregation errors, the spindle assembly checkpoint (SAC) delays anaphase until all sister chromatid pairs have become bipolarly attached. Once microtubules attach to kinetochores, chromosomes are aligned on the metaphase plate, and proper bi-orientation has been achieved, the SAC stopping mechanisms are removed. Entrance into anaphase is mediated by APCCdc20 activation. APCCdc20 is a ubiquitin-protein ligase that tags the protein, securin, for destruction. Securin destruction liberates and activates its bound protease partner, separase. Separase bound to securin remains inhibited; however, when inhibition is r 성인토렌트