• No results found

Diacylglycerol kinase theta and zeta isoforms: regulation of activity, protein binding partners and physiological functions

N/A
N/A
Protected

Academic year: 2021

Share "Diacylglycerol kinase theta and zeta isoforms: regulation of activity, protein binding partners and physiological functions"

Copied!
9
0
0

Bezig met laden.... (Bekijk nu de volledige tekst)

Hele tekst

(1)

Diacylglycerol kinase theta and zeta isoforms: regulation of activity,

protein binding partners and physiological functions

Los, Alrik Pieter

Citation

Los, A. P. (2007, January 25). Diacylglycerol kinase theta and zeta isoforms: regulation of

activity, protein binding partners and physiological functions. Retrieved from

https://hdl.handle.net/1887/9451

Version: Corrected Publisher’s Version

License: Licence agreement concerning inclusion of doctoral thesis in the

Institutional Repository of the University of Leiden

Downloaded from: https://hdl.handle.net/1887/9451

Note: To cite this publication please use the final published version (if applicable).

(2)
(3)
(4)

D i a c y l g l y c e r o l k i n a s e t h e t a a n d z e t a i s o f o r m s : R e g u l a t i o n o f a c t i v i t y, p r o t e i n b i n d i n g p a r t n e r s a n d p h y s i o l o g i c a l f u n c t i o n s

(5)

Design

Crispijn Los J oris S m id t P r int ed b y

P rint P a rt ne rs I psk a m p B .V ., A m st e rd a m

(6)

Diacylglycerol

kinase theta and

zeta isoforms:

Regulation of activity,

protein binding

partners and physio-

logical functions

P roefschrift

ter verkrijging van

de graad van D oc tor aan de U niversiteit Leiden, op gez ag van de R ec tor M agnif ic u s D r. D .D . Breimer,

h oogleraar in de f ac u lteit der W isku nde en N atu u rw etensc h appen en die der G eneesku nde,

volgens b eslu it van h et College voor Promoties te verdedigen op donderdag 2 5 janu ari 2 0 0 7

klokke 1 5 :0 0 u u r

door

A lrik P ieter L os

G eboren te ’s- H ertogenbosch in 1 9 7 5

(7)

P romotiecommissie

Promotor

Prof. Dr. W. H. Moolenaar C o- p romotores

Dr. N. Divecha

Nederlands Kanker Instituut, Amsterdam Dr. W. J. van Blitterswijk

Nederlands Kanker Instituut, Amsterdam R ef erent

Prof. Dr. J. J. Neefjes O v erige l eden

Prof. Dr. P. ten Dijke

T he research described in this thesis was performed at the

Division of Cellular Biochemistry of the Netherlands Cancer Institute, Amsterdam. T his work was supported by the Dutch Cancer Society , grant NK I 2000- 2209 .

Publication of this thesis was financially supported by the Netherlands Cancer Institute and the Dutch Cancer Society .

(8)

7

Contents

Chapter 1

I ntroduction to the signalling functions

of diacylglycerol kinase-c and -e isoforms...9

Chapter 2

S tructure– activity relationship of diacylglycerol

kinase e.

(BBA. 2004 Mar 22;1636(2-3):169-174)

...4 5

Chapter 3

I ntroduction to the family of retinoblastoma

gene products...5 9

Chapter 4

T he retinoblastoma family proteins bind to

and activate diacylglycerol kinase-c

(J BC . 2006 J an 13;28 1(2):8 5 8 -8 66)

...7 5

Chapter 5

Protein kinase

C

inhibits binding of diacylglycerol

kinase-c to the retino blastoma protein

(BBA Mo l e c u l ar C e l l re s e arc h , i n p re s s )

...99

Chapter 6

I s there a role for diacylglycerol kinase-c in cell

cycle regulation? ...1 1 5

Chapter 7

Diacylglycerol kinase-c stimulates muscle

differentiation...1 2 9

S ummary and general discussion...1 4 8

N ederlandse samenvatting...1 5 2

Curriculum V itae...1 5 7

List of Publications...1 5 7

List of Abbreviations...1 5 8

Dankw oord...1 5 9

(9)

Referenties

GERELATEERDE DOCUMENTEN

To find out how this small G protein blocks DGK activity, we individually expressed the regulatory and the catalytic domains of DGK e together with active V 14- R ho A into

In quiescent cells and early in G 1, p107 and p130 in conjugation with E2F4 and E2F5 and chromatin modifying enz ymes bind to E2F -responsive promotors and repress

The retinoblastoma family proteins bind to and activate diacylglycerol kinase-c.. Essential role for nuclear phospholipase C beta 1 in insulin-like growth factor I-induced

Pre-treatment with Ro-31-8220 completely rescued the PMA -mediated inhibition of DGK c binding to p RB (Fig. 1B), indicating that PMA -mediated activation of PKC regulates

In summary, we have shown that cells overexpressing DGK c and DGK c -/- MEF s have similar cell cycle profiles as control cells and that DGK c does not affect p RB - mediated

M yogenin collaborates with M yo D and MEF 2 to regulate ex pression of genes important for terminal differentiation, including myosin heavy chain ( MH C ) and muscle crea-

In this thesis, we provided evidence that DGK c is required for such specific functions, including irradiation-induced cell cycle arrest in p RB -negative cells and in

In dit proefschrift is indirect bewijs gevonden dat DGK c betrokken zou kunnen zijn bij een verstoorde regulatie van de celcyclus in cellen waarin p RB signalering geremd