Regulation of meiotic prophase arrest in mouse oocytes by GPR3, a constitutive activator of the Gs G protein

被引:75
作者
Freudzon, L
Norris, RP
Hand, AR
Tanaka, S
Saeki, Y
Jones, TLZ
Rasenick, MM
Berlot, CH
Mehlmann, LM
Jaffe, LA [1 ]
机构
[1] Univ Connecticut, Ctr Hlth, Dept Cell Biol, Farmington, CT 06032 USA
[2] Univ Connecticut, Ctr Hlth, Dept Pediat Dent, Farmington, CT 06032 USA
[3] Ohio State Univ, Dept Neurol Surg, Columbus, OH 43210 USA
[4] NIDDKD, NIH, Bethesda, MD 20892 USA
[5] Univ Illinois, Dept Physiol & Biophys, Chicago, IL 60612 USA
[6] Univ Illinois, Dept Psychiat, Chicago, IL 60612 USA
[7] Weis Ctr Res, Geisinger Clin, Danville, PA 17822 USA
关键词
D O I
10.1083/jcb.200506194
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
he arrest of meiotic prophase in mouse oocytes within antral follicles requires the G protein G(s) and an orphan member of the G protein-coupled receptor family, GPR3. To determine whether GPR3 activates G(s), the localization of G(alpha s) in follicle-enclosed oocytes from Gpr3(+/+) and Gpr3(-/-) mice was compared by using immunofluorescence and G(alpha s) GFP. GPR3 decreased the ratio of G(alpha s) in the oocyte plasma membrane versus the cytoplasm and also decreased the amount of G(alpha s) in the oocyte. Both of these properties indicate that GPR3 activates G(s). The follicle cells around the oocyte are also necessary to keep the oocyte in prophase, suggesting that they might activate GPR3. However, GPR3-dependent G(s) activity was similar in follicle-enclosed and follicle-free oocytes. Thus, the maintenance of prophase arrest depends on the constitutive activity of GPR3 in the oocyte, and the follicle cell signal acts by a means other than increasing GPR3 activity.
引用
收藏
页码:255 / 265
页数:11
相关论文
共 53 条
[1]   Expression of a green fluorescent protein variant in mouse oocytes by injection of RNA with an added long poly(A) tail [J].
Aida, T ;
Oda, S ;
Awaji, T ;
Yoshida, K ;
Miyazaki, S .
MOLECULAR HUMAN REPRODUCTION, 2001, 7 (11) :1039-1046
[2]   β-adrenergic receptor stimulation promotes Gαs internalization through lipid rafts:: A study in living cells [J].
Allen, JA ;
Yu, JZ ;
Donati, RJ ;
Rasenick, MM .
MOLECULAR PHARMACOLOGY, 2005, 67 (05) :1493-1504
[3]   GAP JUNCTIONS BETWEEN OOCYTE AND COMPANION FOLLICLE CELLS IN MAMMALIAN OVARY [J].
ANDERSON, E ;
ALBERTINI, DF .
JOURNAL OF CELL BIOLOGY, 1976, 71 (02) :680-686
[4]   Identification of signal transduction pathways used by orphan G protein-coupled receptors [J].
Bresnick, JN ;
Skynner, HA ;
Chapman, KL ;
Jack, AD ;
Zamiara, E ;
Negulescu, P ;
Beaumont, K ;
Patel, S ;
McAllister, G .
ASSAY AND DRUG DEVELOPMENT TECHNOLOGIES, 2003, 1 (02) :239-249
[5]   A monomeric red fluorescent protein [J].
Campbell, RE ;
Tour, O ;
Palmer, AE ;
Steinbach, PA ;
Baird, GS ;
Zacharias, DA ;
Tsien, RY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (12) :7877-7882
[6]   INHIBITORY EFFECT OF DIBUTYRYL CAMP ON MOUSE OOCYTE MATURATION IN-VITRO [J].
CHO, WK ;
STERN, S ;
BIGGERS, JD .
JOURNAL OF EXPERIMENTAL ZOOLOGY, 1974, 187 (03) :383-386
[7]   Role of cyclic nucleotide signaling in oocyte maturation [J].
Conti, M ;
Andersen, CB ;
Richard, F ;
Mehats, C ;
Chun, SY ;
Horner, K ;
Jin, C ;
Tsafriri, A .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2002, 187 (1-2) :153-159
[8]   G2 arrest in Xenopus oocytes depends on phosphorylation of cdc25 by protein kinase A [J].
Duckworth, BC ;
Weaver, JS ;
Ruderman, JV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (26) :16794-16799
[9]   MOLECULAR-CLONING OF AN ORPHAN G-PROTEIN-COUPLED RECEPTOR THAT CONSTITUTIVELY ACTIVATES ADENYLATE-CYCLASE [J].
EGGERICKX, D ;
DENEF, JF ;
LABBE, O ;
HAYASHI, Y ;
REFETOFF, S ;
VASSART, G ;
PARMENTIER, M ;
LIBERT, F .
BIOCHEMICAL JOURNAL, 1995, 309 :837-843