QUANTITATIVE CHANGES IN CYTOSKELETAL BETA-ACTIN AND GAMMA-ACTIN MESSENGER-RNAS AND APPARENT ABSENCE OF SARCOMERIC ACTIN GENE TRANSCRIPTS IN EARLY MOUSE EMBRYOS

被引:44
作者
TAYLOR, KD
PIKO, L
机构
[1] VET ADM MED CTR,DEV BIOL LAB,151-B3,SEPULVEDA,CA 91343
[2] CALTECH,DIV BIOL,PASADENA,CA 91125
关键词
Actin isoforms; Developmental regulation; Gene expression; Preimplantation development;
D O I
10.1002/mrd.1080260204
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Actin is known to be synthesized both during oogenesis and in cleavage‐stage embryos in mice. Cytoskeletal β‐actin appears to be the major component, followed by γ‐actin, but the synthesis of α‐actin has also been inferred from protein electrophoretic patterns. We have studied the expression of cytoskeletal (β‐ and γ‐) and sarcomeric (α‐cardiac and α‐skeletal) actin genes at the level of the individual mRNAs in blot hybridization experiments using isoform‐specific RNA probes. The results show that there are about 2 × 104 β‐actin mRNA molecules in the fully grown oocyte; this number drops to about one‐half in the egg and less than one‐tenth in the late two‐cell embryo but increases rapidly during cleavage to about 3 × 105 molecules in the late blastocyst. The amount of γ‐actin mRNA is similar to that of β‐actin in oocytes and eggs but only about 40% as much in late blastocysts, indicating a differential accumulation of these mRNAs during cleavage. The developmental pattern of β‐ and γ‐actin mRNA provides a striking example of the transition from maternal to embryonic control that occurs at the two‐cell stage and involves the elimination of most or all of the maternal actin mRNA. There was no detectable α‐cardiac or α‐skeletal mRNA (i.e., < 1,000 molecules per embryo) at any stage from oocyte to late blastocyst, suggesting that the sarcomeric actin genes are silent during preimplantation development. Copyright © 1990 Wiley‐Liss, Inc.
引用
收藏
页码:111 / 121
页数:11
相关论文
共 58 条
[31]  
MARO B, 1984, J EMBRYOL EXP MORPH, V81, P211
[32]  
MELTON DA, 1984, NUCLEIC ACIDS RES, V12, P7035, DOI 10.1093/nar/12.18.7035
[33]   A FETAL SKELETAL-MUSCLE ACTIN MESSENGER-RNA IN THE MOUSE AND ITS IDENTITY WITH CARDIAC ACTIN MESSENGER-RNA [J].
MINTY, AJ ;
ALONSO, S ;
CARAVATTI, M ;
BUCKINGHAM, ME .
CELL, 1982, 30 (01) :185-192
[34]   NUMBER AND ORGANIZATION OF ACTIN-RELATED SEQUENCES IN THE MOUSE GENOME [J].
MINTY, AJ ;
ALONSO, S ;
GUENET, JL ;
BUCKINGHAM, ME .
JOURNAL OF MOLECULAR BIOLOGY, 1983, 167 (01) :77-101
[35]   CELL TYPE-SPECIFIC ACTIVATION OF ACTIN GENES IN THE EARLY AMPHIBIAN EMBRYO [J].
MOHUN, TJ ;
BRENNAN, S ;
DATHAN, N ;
FAIRMAN, S ;
GURDON, JB .
NATURE, 1984, 311 (5988) :716-721
[36]   IDENTIFICATION AND QUANTIFICATION OF ACTIN ISOFORMS IN VERTEBRATE CELLS AND TISSUES [J].
OTEY, CA ;
KALNOSKI, MH ;
BULINSKI, JC .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1987, 34 (02) :113-124
[37]   QUANTITATION OF PARAMETERS THAT DETERMINE RATE OF OVALBUMIN SYNTHESIS [J].
PALMITER, RD .
CELL, 1975, 4 (03) :189-197
[38]   CHANGES IN STATE OF ADENYLATION AND TIME COURSE OF DEGRADATION OF MATERNAL MESSENGER-RNAS DURING OOCYTE MATURATION AND EARLY EMBRYONIC-DEVELOPMENT IN THE MOUSE [J].
PAYNTON, BV ;
REMPEL, R ;
BACHVAROVA, R .
DEVELOPMENTAL BIOLOGY, 1988, 129 (02) :304-314
[39]   OOCYTE-SPECIFIC EXPRESSION AND DEVELOPMENTAL REGULATION OF ZP3, THE SPERM RECEPTOR OF THE MOUSE ZONA-PELLUCIDA [J].
PHILPOTT, CC ;
RINGUETTE, MJ ;
DEAN, J .
DEVELOPMENTAL BIOLOGY, 1987, 121 (02) :568-575
[40]   AMOUNTS, SYNTHESIS, AND SOME PROPERTIES OF INTRACISTERNAL A PARTICLE-RELATED RNA IN EARLY MOUSE EMBRYOS [J].
PIKO, L ;
HAMMONS, MD ;
TAYLOR, KD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (02) :488-492