Mad1 is a non-essential protein which in yeast has a function in the spindle assembly checkpoint (SAC). This checkpoint monitors chromosome attachment to spindle microtubules and prevents cells from starting anaphase until the spindle is built up. The name Mad refers to the observation that mutant cells are mitotic arrest deficient (MAD) during microtubule depolymerization. Mad1 recruits the anaphase inhibitor Mad2 to unattached kinetochores and is essential for Mad2-Cdc20 complex formation in vivo but not in vitro. In vivo, Mad1 acts as a competitive inhibitor of the Mad2-Cdc20 complex. Mad1 is phosphorylated by Mps1 which then leads together with other activities to the formation of the mitotic checkpoint complex (MCC). Thereby it inhibits the activity of the anaphase-promoting complex/cyclosome (APC/C). Homologues of Mad1 are conserved in eukaryotes from yeast to mammals.
Introduction
In the early 90s, yeast genes were identified which mutations resulted in a defect in mitotic arrest in response to microtubule disassembly (mitotic arrest deficient genes - MAD genes). These cells showed no mitotic arrest in the presence of microtubule polymerization inhibitors and were therefore not able to delay cell division. The genes identified included the MAD1, MAD2 and MAD3 genes. They are conserved in all eukaryotes and are involved in a pathway that is active in prometaphase to prevent the premature separation of sister chromatids and constitute the so-called spindle assembly checkpoint (SAC). This checkpoint monitors the status of chromosome attachment to the mitotic spindle and inhibits the metaphase to anaphase transition by preventing the activation of the anaphase-promoting complex/cyclosome (APC/C), and thereby the degradation of cell cycle regulators. Mad1 is in this pathway accumulated at unattached kinetochores and acts as a sensor for unattached kinetochores in this machinery.
Function
Eukaryotic cells show a mitotic arrest in the presence of microtubule polymerization inhibitors. A spindle assembly checkpoint monitors the status of the spindle and links the metaphase-anaphase transition to proper bipolar attachment of all kinetochores to the mitotic spindle. The spindle assembly checkpoint inhibits the activity of the anaphase promoting complex by preventing degradation of downstream effectors, which otherwise lead to anaphase onset and exit from mitosis. Depletion of Mad1 leads to the loss of SAC function. Mad1 localises predominantly at unattached kinetochores and triggers mitotic arrest in case of a single unattached kinetochore. Mad1 recruits the important SAC component Mad2 to unattached kinetochores and induces mitotic arrest signal amplification. There is a pool of free cytoplasmic Mad2 in its inactive open conformation called o-MAD2. When bound to Mad1, Mad2 adopts an active conformation called closed (c-Mad2) and forms a heterotetramer of two Mad1 and two c-Mad2 units. The heterotetramer of Mad1–c-Mad2 is very stable and works as a catalytic receptor for free cytoplasmic o-Mad2. Free o-Mad2 binds to this receptor and changes its conformation to the active closed form. This second c-MAD2 is transferred to Cdc20 with yet unknown mechanism and forms Cdc20–c-Mad2 complex. This complex is an essential component of mitotic checkpoint complex (MCC). MCC binds and inhibits APC/C and therefore arrests progression through mitosis.
Regulation
There are two upstream checkpoint kinases implicated in regulating Mad1 function through phosphorylation. Mps1 phosphorylates Mad1 both in vitro and in vivo and is thought to regulate Mad1 and Mad2 localization to kinetochores and their interaction dynamics. BUB1 is the other kinase that recruits Mad1 to kinetochores and activates it if a kinetochore is unattached. If a kinetochore is attached to spindle, SAC inhibitor p31comet inhibits Mad1 mediated conformational rearrangement of Mad2 and prevents Mad2 from binding to Cdc20.