All organisms must transmit genetic information to offspring through cell division, and mitotic spindle participates in the process. Spindle dynamics through depolymerization or polymerization of microtubules generates the driving force required for chromosome movements in mitosis. To date, studies have shown that microtubule arrays control the directions of cell division and diverse microtubule-associated proteins regulate cell division. But a clear picture of how microtubules and microtubule-associated proteins modulate cell division remains unknown. Depletion of end-binding protein 1 by RNA-mediated inhibition shows that one of the microtubule-associated proteins, end-binding protein 1, plays a crucial role in mitotic spindle formation and promotes microtubule dynamics and is needed for the proper segregation of mitotic chromosomes during anaphase in Drosophila cells. Here, we review the properties of end-binding protein 1 and the roles of end-binding protein 1 in regulating microtubule behavior and in cell cycle. 2115 namic properties of microtubules. Microtubules (MTs) are dynamic hollow tubes comprising α, β-tubulin dimers that disassemble and reassemble at two ends: the slow-growing (minus) and fast-growing (plus) ends. It is now widely known that MT behavior is modulated by a number of MT-associated proteins (MAPs), which can influence dynamic instability parameters and consequently impact on mitotic progression and fidelity. Many of these MAPs share the ability to recognize only the distal part of a polymerizing MT, known as the MT plus end. For this reason, these MAPs are currently known as MT plus-end-tracking proteins (+TIPs) [1] [2]. Recently, +TIPs have emerged as regulators of MT dynamics. The plus end explores the cell periphery and shows dynamic instability, switching rapidly between the two phases of growth and shrinkage. Thus this dynamic scaffold performs a variety of very different functions. Genetic and biochemical studies have shown that +TIPs interact with each other and form protein complexes [3].End-binding protein 1 (EB1) promotes MT polymerization and interacts directly with many other +TIPs and cytoskeletal proteins such as cytoplasmic linker protein 170 (CLIP-170) and the dynactin large subunit p150 Glued , and mitotic centromere-associated kinesin, microtubule-actin crosslinking factor and adenomatous polyposis coli (APC) [4] [5]. Thus, EB1 has been proposed to form the core of the microtubule plus-end complex and act as a hub in interactions with +TIPs [6] [7].Division of one cell into two genetically identical daughter cells occurs through two coordinated processes which are known as mitosis (division of the nucleus) and cytokinesis (division of the cytoplasm). The transition from interphase to mitosis involves a dramatic reorganization of the MT cytoskeleton. In fact, there is an increase in MT dynamics which occurs concomitantly with NEB that could be important for spindle morphogenesis [8] [9]. Studies have shown that accurate segregation of the replicated genome during cell...