Expression of the rig gene in mouse oocytes and early embryos

A clone selected from a two‐cell mouse embryo cDNA library has been sequenced and identified as rig cDNA. The rig gene codes for a highly conserved nuclear protein, which may have a general role in cell growth or replication (Shiga et al.: Proc Natl Acad Sci USA 87:3594, 1990). The quantitative changes in rig mRNA were studied in blot hybridization experiments with total RNA from oocytes and early embryos. The amount and relative abundance of rig mRNA change considerably during early development. There are about 1.6 × 104 rig mRNA molecules in a late growth‐stage oocyte; this number is reduced to about one‐tenth in the ovulated egg but increases about twenty‐fold during cleavage through the blastocyst stage. In F9 embryonal carcinoma cells, the relative abundance of rig mRNA is similar to that in blastocysts (about 0.1% of the mRNA population), but it is about eight‐fold higher in the mouse myeloma cell line MOPC‐104E. The high level of rig mRNA in late growth‐stage oocytes suggests that the rig gene product may be important for cverall transcriptional activity rather than DNA replication and mitosis. Alternatively, the rig protein may be a storage product of oogenesis and have a role in the initiation of development.

[1]  L. Pikó,et al.  Quantitative changes in cytoskeletal β‐ and γ‐actin mRNAS and apparent absence of sarcomeric actin gene transcripts in early mouse embryos , 1990 .

[2]  H. Okamoto,et al.  Isolation and characterization of the human homologue of rig and its pseudogenes: the functional gene has features characteristic of housekeeping genes. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[3]  H. Yamamoto,et al.  Nucleotide sequence determination of mouse, chicken and Xenopus laevis rig cDNAs: the rig-encoded protein is extremely conserved during vertebrate evolution. , 1990, Biochemical and biophysical research communications.

[4]  R. Rickles,et al.  Regulated polyadenylation controls mRNA translation during meiotic maturation of mouse oocytes. , 1989, Genes & development.

[5]  P. Wassarman,et al.  Gene expression during mammalian oogenesis and early embryogenesis: quantification of three messenger RNAs abundant in fully grown mouse oocytes. , 1989, Development.

[6]  R. Rempel,et al.  Changes in state of adenylation and time course of degradation of maternal mRNAs during oocyte maturation and early embryonic development in the mouse. , 1988, Developmental biology.

[7]  R. Rickles,et al.  Antisense RNA directed against the 3' noncoding region prevents dormant mRNA activation in mouse oocytes. , 1988, Science.

[8]  S. Takasawa,et al.  Expression of the insulinoma gene rig during liver regeneration and in primary cultured hepatocytes. , 1988, Biochemical and biophysical research communications.

[9]  J. Browse,et al.  Double stranded DNA sequencing as a choice for DNA sequencing. , 1988, Nucleic acids research.

[10]  D. Belin,et al.  Meiotic maturation of mouse oocytes triggers the translation and polyadenylation of dormant tissue-type plasminogen activator mRNA. , 1987, Genes & development.

[11]  L. Pikó,et al.  Patterns of mRNA prevalence and expression of B1 and B2 transcripts in early mouse embryos. , 1987, Development.

[12]  H. Yamamoto,et al.  Evolutionary conservation of the insulinoma gene rig and its possible function. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[13]  L. Pikó,et al.  Amounts of mitochondrial DNA and abundance of some mitochondrial gene transcripts in early mouse embryos. , 1987, Developmental biology.

[14]  J. Dean,et al.  Oocyte-specific expression and developmental regulation of ZP3, the sperm receptor of the mouse zona pellucida. , 1987, Developmental biology.

[15]  G. Schultz MOLECULAR BIOLOGY OF ThE EARLY MOUSE EMBRYO , 1986 .

[16]  H. Yamamoto,et al.  Novel Gene Activated in Rat Insulinomas , 1986, Diabetes.

[17]  J. J. Lee,et al.  Activation of sea urchin actin genes during embryogenesis. Measurement of transcript accumulation from five different genes in Strongylocentrotus purpuratus. , 1986, Journal of molecular biology.

[18]  M. Wagner A consideration of the origin of processed pseudogenes , 1986 .

[19]  M. Johnson,et al.  The relationship between cleavage, DNA replication, and gene expression in the mouse 2-cell embryo. , 1984, Journal of embryology and experimental morphology.

[20]  L. Pikó,et al.  Amounts, synthesis, and some properties of intracisternal A particle-related RNA in early mouse embryos. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[21]  Andrew D. Johnson,et al.  Half-lives and relative amounts of stored and polysomal ribosomes and poly(A) + RNA in mouse oocytes. , 1983, Developmental biology.

[22]  L. Pikó,et al.  Poly(A) length, cytoplasmic adenylation and synthesis of poly(A)+ RNA in early mouse embryos. , 1983, Developmental biology.

[23]  P. Braude,et al.  The transition from maternal to embryonic control in the 2‐cell mouse embryo. , 1982, The EMBO journal.

[24]  L. Pikó,et al.  Quantitative changes in total RNA, total poly(A), and ribosomes in early mouse embryos. , 1982, Developmental biology.

[25]  L. Pikó,et al.  RNA synthesis and cytoplasmic polyadenylation in the one-cell mouse embryo , 1982, Nature.

[26]  E. Adamson,et al.  Cell interactions modulate embryonal carcinoma cell differentiation into parietal or visceral endoderm , 1981, Nature.