Minus-end capture of preformed kinetochore fibers contributes to spindle morphogenesis

نویسندگان

  • Alexey Khodjakov
  • Lily Copenagle
  • Michael B. Gordon
  • Duane A. Compton
  • Tarun M. Kapoor
چکیده

Near-simultaneous three-dimensional fluorescence/differential interference contrast microscopy was used to follow the behavior of microtubules and chromosomes in living alpha-tubulin/GFP-expressing cells after inhibition of the mitotic kinesin Eg5 with monastrol. Kinetochore fibers (K-fibers) were frequently observed forming in association with chromosomes both during monastrol treatment and after monastrol removal. Surprisingly, these K-fibers were oriented away from, and not directly connected to, centrosomes and incorporated into the spindle by the sliding of their distal ends toward centrosomes via a NuMA-dependent mechanism. Similar preformed K-fibers were also observed during spindle formation in untreated cells. In addition, upon monastrol removal, centrosomes established a transient chromosome-free bipolar array whose orientation specified the axis along which chromosomes segregated. We propose that the capture and incorporation of preformed K-fibers complements the microtubule plus-end capture mechanism and contributes to spindle formation in vertebrates.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Kinetochore-driven formation of kinetochore fibers contributes to spindle assembly during animal mitosis

It is now clear that a centrosome-independent pathway for mitotic spindle assembly exists even in cells that normally possess centrosomes. The question remains, however, whether this pathway only activates when centrosome activity is compromised, or whether it contributes to spindle morphogenesis during a normal mitosis. Here, we show that many of the kinetochore fibers (K-fibers) in centrosoma...

متن کامل

Mechanisms for focusing mitotic spindle poles by minus end–directed motor proteins

During the formation of the metaphase spindle in animal somatic cells, kinetochore microtubule bundles (K fibers) are often disconnected from centrosomes, because they are released from centrosomes or directly generated from chromosomes. To create the tightly focused, diamond-shaped appearance of the bipolar spindle, K fibers need to be interconnected with centrosomal microtubules (C-MTs) by mi...

متن کامل

The other side of kinetochore fibers

The other side of kinetochore fibers n page 671, Khodjakov et al. uncover a new mechanism of spindle morphogenesis that involves the capture of microtubule minus ends. In the established model of spindle formation in vertebrate cells, spindle microtubule minus ends are focused at spindle poles in association with centrosome-nucleated microtubules. Kinetochore O fibers, which pull chromosomes to...

متن کامل

Phosphorylation cycles on vesicles

The other side of kinetochore fibers n page 671, Khodjakov et al. uncover a new mechanism of spindle morphogenesis that involves the capture of microtubule minus ends. In the established model of spindle formation in vertebrate cells, spindle microtubule minus ends are focused at spindle poles in association with centrosome-nucleated microtubules. Kinetochore O fibers, which pull chromosomes to...

متن کامل

Properties of the kinetochore in vitro. II. Microtubule capture and ATP- dependent translocation

We have studied the interaction of preformed microtubules (MTs) with the kinetochores of isolated chromosomes. This reaction, which we call MT capture, results in MTs becoming tightly bound to the kinetochore, with their ends capped against depolymerization. These observations, combined with MT dynamic instability, suggest a model for spindle morphogenesis. In addition, ATP appears to mobilize ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • The Journal of Cell Biology

دوره 160  شماره 

صفحات  -

تاریخ انتشار 2003