Isolation of microtubules and a dynein-like MgATPase from unfertilized sea urchin eggs
- PMID: 6144678
Isolation of microtubules and a dynein-like MgATPase from unfertilized sea urchin eggs
Abstract
Taxol was used to prepare microtubules from unfertilized eggs of sea urchins Lytechinus pictus, Strongylocentrotus droebachiensis , and Strongylocentrotus purpuratus. By electron microscopy, these microtubules possessed normal morphology and were decorated with projections. The polypeptides present were tubulin plus microtubule-associated proteins (MAPs) which included various high molecular weight polypeptides, and a Mr = 80,000 polypeptide. These MAPs were extracted from the microtubules by differential centrifugation in high ionic strength buffers, yielding a pellet of microtubules which were not decorated with projections. The Mr = 80,000 and high molecular weight MAPs were separated using Bio-Gel A-1.5 m chromatography, and shown to bind taxol-stabilized microtubules assembled from purified bovine brain tubulin. A dynein-like MgATPase activity is present in sea urchin egg extracts. 10-20% of this MgATPase co-pelleted with the taxol-assembled microtubules, under conditions where greater than 90% of the tubulin pelleted. During subsequent fractionation of the microtubules, by (i) high salt extraction followed by gel filtration or sucrose density gradient fractionation or (ii) ATP extraction, the MgATpase co-purified with high Mr MAPs. The MgATPase which remained in the microtubule-depleted egg extract was partially purified by (NH4)2SO4 fractionation, followed by Bio-Gel A-5 m and hydroxylapatite chromatography. The high Mr MAP MgATPase and the hydroxylapatite MgATPase both contained a prominent polypeptide (Mr approximately 350,000), which co-migrated on sodium dodecyl sulfate gels with the major heavy chain of dynein extracted from sperm axonemes. Our data suggest that this Mr approximately 350,000 polypeptide is cytoplasmic dynein.
Similar articles
-
A latent activity dynein-like cytoplasmic magnesium adenosine triphosphatase.J Biol Chem. 1985 Jan 25;260(2):699-702. J Biol Chem. 1985. PMID: 3155728
-
Dynein isoforms in sea urchin eggs.J Biol Chem. 1988 May 15;263(14):6759-71. J Biol Chem. 1988. PMID: 2896199
-
A microtubule-activated ATPase from sea urchin eggs, distinct from cytoplasmic dynein and kinesin.Proc Natl Acad Sci U S A. 1986 Jul;83(13):4799-803. doi: 10.1073/pnas.83.13.4799. Proc Natl Acad Sci U S A. 1986. PMID: 2873571 Free PMC article.
-
Quantitation of the dynein pool in unfertilized sea urchin eggs.Biochim Biophys Acta. 1989 Jan 27;990(1):31-9. doi: 10.1016/s0304-4165(89)80008-x. Biochim Biophys Acta. 1989. PMID: 2521562
-
Characterization of the sea-urchin egg microtubule-activated ATPase.J Cell Sci Suppl. 1986;5:197-204. doi: 10.1242/jcs.1986.supplement_5.13. J Cell Sci Suppl. 1986. PMID: 2958488
Cited by
-
Sequence and submolecular localization of the 115-kD accessory subunit of the heterotrimeric kinesin-II (KRP85/95) complex.J Cell Biol. 1996 Feb;132(3):371-80. doi: 10.1083/jcb.132.3.371. J Cell Biol. 1996. PMID: 8636215 Free PMC article.
-
Identification of a novel force-generating protein, kinesin, involved in microtubule-based motility.Cell. 1985 Aug;42(1):39-50. doi: 10.1016/s0092-8674(85)80099-4. Cell. 1985. PMID: 3926325 Free PMC article.
-
Characterization of the microtubule-activated ATPase of brain cytoplasmic dynein (MAP 1C).J Cell Biol. 1988 Sep;107(3):1001-9. doi: 10.1083/jcb.107.3.1001. J Cell Biol. 1988. PMID: 2971069 Free PMC article.
-
Analysis of cytoskeletal and motility proteins in the sea urchin genome assembly.Dev Biol. 2006 Dec 1;300(1):219-37. doi: 10.1016/j.ydbio.2006.08.052. Epub 2006 Aug 26. Dev Biol. 2006. PMID: 17027957 Free PMC article.
-
A monoclonal antibody to a mitotic microtubule-associated protein blocks mitotic progression.J Cell Biol. 1990 Aug;111(2):511-22. doi: 10.1083/jcb.111.2.511. J Cell Biol. 1990. PMID: 2199459 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous