Microtubule assembly and turnover in growing axons.
نویسندگان
چکیده
We have shown previously that axonal microtubules (MTs) are composite, consisting of two distinct domains that differ in their content of tyrosinated alpha-tubulin (tyr-tub). One domain is poor in tyr-tub and is situated at the minus end of the MT. The other domain is rich in tyr-tub and extends from the plus end of the tyr-tub-poor domain to the end of the MT. We have proposed that the spatial variation in the relative content of tyr-tub along individual MTs reflects corresponding variations in their dynamic properties. The present experiments have tested this hypothesis directly by microinjecting biotin-labeled tubulin (Bt-tub) into cultured sympathetic neurons and then quantifying the appearance of Bt-tub in the tyr-tub-rich and tyr-tub-poor polymer of the axon. Bt-tub appeared in axonal MTs with a half-life (t1/2) of approximately 2.2 hr. This time course reflected an average of two distinct components corresponding to the tyr-tub-rich and tyr-tub-poor polymer that had apparent t1/2 values of approximately 1.3 and 3.3 hr, respectively. In individual MTs, Bt-tub first appeared in the tyr-tub-rich domain and then only later appeared in the tyr-tub-poor domain. Also, the appearance of Bt-tub in the tyr-tub-rich polymer typically began precisely at its origin from the tyr-tub-poor domain, indicating that the tyr-tub-poor polymer is assembly-competent and nucleates the assembly of tyr-tub-rich polymer locally within the axon. The stability properties of axonal MTs are discussed in terms of organizing MT assembly locally in the axon and generating long MTs for growing long axons.
منابع مشابه
Tau is enriched on dynamic microtubules in the distal region of growing axons.
It is widely held that tau determines the stability of microtubules in growing axons, although direct evidence supporting this hypothesis is lacking. Previous studies have shown that the microtubule polymer in the distal axon and growth cone is the most dynamic of growing axons; it turns over more rapidly and is more sensitive to microtubule depolymerizing drugs than the polymer situated proxim...
متن کاملP 97: Neurodegeneration Induced by Tau protein
Tau is one of several types of microtubule-associated proteins (MAPs), responsible for the assembly and stability of microtubule networks that is present only in neurons and predominantly localized in axons which its functions are tightly regulated by phosphorylation. Via as yet unknown mechanisms, tau becomes hyperphosphorylated and accompanies with neuronal degeneration, loss of synapses...
متن کاملMicrotubule transport and assembly during axon growth
There is controversy concerning the mechanisms by which the axonal microtubule (MT) array is elaborated, with some models focusing on MT assembly and other models focusing on MT transport. We have proposed a composite model in which MT assembly and transport are both important (Joshi, H.C., and P.W. Baas. 1993. J. Cell Biol. 121:1191-1196). In the present study, we have taken a novel approach t...
متن کاملAcute inactivation of tau has no effect on dynamics of microtubules in growing axons of cultured sympathetic neurons.
Tau is a developmentally regulated microtubule (MT)-associated protein in neurons that has been implicated in neuronal morphogenesis. On the basis of test tube studies, tau has been proposed to function in axon growth by stabilizing MTs and thereby promoting MT assembly. We have tested this hypothesis by examining the effects of acute inactivation of tau on axonal MTs. Tau was inactivated by mi...
متن کاملKinesin-5 is a microtubule polymerase
Kinesin-5 slides antiparallel microtubules during spindle assembly, and regulates the branching of growing axons. Besides the mechanical activities enabled by its tetrameric configuration, the specific motor properties of kinesin-5 that underlie its cellular function remain unclear. Here by engineering a stable kinesin-5 dimer and reconstituting microtubule dynamics in vitro, we demonstrate tha...
متن کاملذخیره 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 ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The Journal of neuroscience : the official journal of the Society for Neuroscience
دوره 16 2 شماره
صفحات -
تاریخ انتشار 1996