REGULATION OF SPINDLE MICROTUBULE ASSEMBLY-DISASSEMBLY: LOCALIZATION AND POSSIBLE FUNCTIONAL ROLE OF CALCIUM DEPENDENT REGULATOR PROTEIN

1978 ◽  
pp. 299-314 ◽  
Author(s):  
B.R. Brinkley ◽  
J.M. Marcum ◽  
M.J. Welsh ◽  
J.R. Dedman ◽  
A.R. Means
1979 ◽  
Author(s):  
S.N. Levine ◽  
A.L. Steiner ◽  
G.C. White

Calcium-dependent regulator protein (CDR) is a 17,000 molecular weight polypeptide which has been demonstrated in a number of mammalian cells and has been shown to 1) modulate activation of adenylate cyclase activity, 2) stimulate erythrocyte membrane (Ca++/Mg++) ATPase activity, 3) stimulate cardiac microsomal calcium uptake, 4) activate smooth muscle myosin light chain kinase activity, and 5) regulate microtubule assembly and disassembly. Because of the role of CDR in calcium metabolism and contractile protein function, we have examined the presence and subcellular distribution of this protein in preparations of human platelets. CDR was quantified using a two-step phosphodiesterase assay (Kakiuchi et al, PNAS 70:3526, 1973). Bovine brain CDR which was homogeneous by SDS polyacrylamide gel electrophoresis was used as a standard. Whole platelets contained approximately 4.4 ug CDR/mg platelet protein. When platelets were fractionated by glycerol osmoticlysis followed by separation on 27% sucrose, the soluble portion had the highest specific activity and the membrane fraction, the lowest. These studies demonstrate the presence of CDR in platelets and indicate subcellular compart-mentalization of the protein. The role of CDR in calcium metabolism and contractile protein function in platelets is currently under study, (AHA 78-1215/NIH AM17438, DE02668)


1980 ◽  
Vol 126 (1) ◽  
pp. 1-13 ◽  
Author(s):  
Charles D. Hebert ◽  
W.L. Steffens ◽  
John J. Wille

Development ◽  
1983 ◽  
Vol 77 (1) ◽  
pp. 15-37
Author(s):  
Geertje A. Ubbels ◽  
K. Hara ◽  
C. H. Koster ◽  
M. W. Kirschner

A normal table of events of the first cleavage period in the fertilized egg (cf. Gerhart, 1980) has been completed (cf. Table I) by studying external and internal features. Through a cytological study of eggs fixed after video time-lapse observation such featurescan directly be correlated and it has been shown that the first postfertilization wave (PFW) reflects spermaster growth, which causes rearrangements of animal yolk material. Thismay, in conjunction with the interaction of the spermaster rays with the cortex, define, in time as well as in space, the asymmetric cortical contraction which we suppose to evoke asymmetry in the animal hemisphere by formation of the vitelline wall (Pasteels, 1964) and in the vegetal hemisphere by formation of the Vegetal Dorsalising Centre (Kirschneret al. 1981). Neither prick-activated eggs nor fertilized eggs incubated in vinblastine develop a spermaster. Under these conditions abnormal cytoplasmic segregation may be directed by gravity alone. For normal development the activated egg must in some way, for instance through the sperm centriole, organize microtubule assembly into a monaster. The centriole actsas a microtubule-organizing centre in structuring the egg's cytoskeleton, and through this directs localization of the various yolk components, in time as well as in space. In egg rotation experiments performed under appropriate conditions, the cytoskeleton is disturbed and yolk rearranges under gravity till a new equilibrium is established which determines a new dorsoventral polarity. Such experiments also show that neither the dorsal cytoplasm nor the grey crescent cortex act as the ultimate dorsal determinants, since their localization is unaltered upon rotation, whereas the overall yolk distribution is significantly changed.


2019 ◽  
Author(s):  
Junming Sun ◽  
Kuiqing Cui ◽  
Zhipeng Li ◽  
Bangjun Gao ◽  
Jianrong Jiang ◽  
...  

Abstract Acetylated microtubule improves porcine oocyte microtubule structure, meiotic maturation and subsequent embryonic development. HDAC6 can specifically deacetylate α-tubulin in assembled microtubules, increased acetylated microtubule treatment with tubacin, a HDAC6-selective inhibitor, is beneficial for porcine oocytes maturation and early embryogenesis. Here it is shown that α-tubulin acetylation gradually decreased from MI to IVF pronuclear stage. The increased acetylation of α-tubulin significantly reduced the abnormal rate of microtubules, furthermore, the proportion of mitochondria in the vicinity of IVF nucleus was significantly enhanced in MI and MII stages. The expression levels of microtubule assembly genes ( TUBA1A , α TAT1 and MAP2 ) significantly up-regulated in MI and MII stages. In addition, the oocytes with high acetylation level of α-tubulin significantly improved maturation, syngamy and IVF blastocyst formation compared with the control oocytes. In present study, these indicate functional role of increased acetylated α-tubulin advances normal spindle formation and mitochondrial concentration, moreover, improves porcine maturation, syngamy and preimplantation embryo development.


1978 ◽  
Vol 75 (8) ◽  
pp. 3771-3775 ◽  
Author(s):  
J. M. Marcum ◽  
J. R. Dedman ◽  
B. R. Brinkley ◽  
A. R. Means

2009 ◽  
Vol 221 (03) ◽  
Author(s):  
B Steiger ◽  
I Leuschner ◽  
D Denkhaus ◽  
D von Schweinitz ◽  
T Pietsch
Keyword(s):  

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