pS2 gene especially expressed in the late G1/S phase of mouse astrocytes. 1994

M Hirota, and S Miyashita, and H Hayashi, and Y Furukawa, and K Hayashi
Department of Molecular Biology, Gifu Pharmaceutical University, Japan.

By the reverse transcription-polymerase chain reaction we investigated the localization of pS2 mRNA, which encodes a secreted polypeptide of 60 amino acids with unknown function, in the adult mouse. This method revealed that the expression of pS2 mRNA was not restricted to the stomach as previously reported but was also found in various other tissues such as brain, heart, spleen, and muscle. The pS2 mRNA was additionally detected in astrocytes cultured from the whole brain of the newborn mouse. The pS2 expression in these astrocytes increased with cell growth and sharply declined after the cells reached the stationary phase. In the cells synchronized by the serum deprivation-refeeding technique, the expression of pS2 mRNA was only found at late G1 and S phase. These results suggest that the transcripts of pS2 gene are widely distributed throughout the entire body of the mouse and that they play some important cell cycle-related role in these tissues.

UI MeSH Term Description Entries
D007399 Interphase The interval between two successive CELL DIVISIONS during which the CHROMOSOMES are not individually distinguishable. It is composed of the G phases (G1 PHASE; G0 PHASE; G2 PHASE) and S PHASE (when DNA replication occurs). Interphases
D009363 Neoplasm Proteins Proteins whose abnormal expression (gain or loss) are associated with the development, growth, or progression of NEOPLASMS. Some neoplasm proteins are tumor antigens (ANTIGENS, NEOPLASM), i.e. they induce an immune reaction to their tumor. Many neoplasm proteins have been characterized and are used as tumor markers (BIOMARKERS, TUMOR) when they are detectable in cells and body fluids as monitors for the presence or growth of tumors. Abnormal expression of ONCOGENE PROTEINS is involved in neoplastic transformation, whereas the loss of expression of TUMOR SUPPRESSOR PROTEINS is involved with the loss of growth control and progression of the neoplasm. Proteins, Neoplasm
D011506 Proteins Linear POLYPEPTIDES that are synthesized on RIBOSOMES and may be further modified, crosslinked, cleaved, or assembled into complex proteins with several subunits. The specific sequence of AMINO ACIDS determines the shape the polypeptide will take, during PROTEIN FOLDING, and the function of the protein. Gene Products, Protein,Gene Proteins,Protein,Protein Gene Products,Proteins, Gene
D001921 Brain The part of CENTRAL NERVOUS SYSTEM that is contained within the skull (CRANIUM). Arising from the NEURAL TUBE, the embryonic brain is comprised of three major parts including PROSENCEPHALON (the forebrain); MESENCEPHALON (the midbrain); and RHOMBENCEPHALON (the hindbrain). The developed brain consists of CEREBRUM; CEREBELLUM; and other structures in the BRAIN STEM. Encephalon
D001923 Brain Chemistry Changes in the amounts of various chemicals (neurotransmitters, receptors, enzymes, and other metabolites) specific to the area of the central nervous system contained within the head. These are monitored over time, during sensory stimulation, or under different disease states. Chemistry, Brain,Brain Chemistries,Chemistries, Brain
D001973 Bromodeoxyuridine A nucleoside that substitutes for thymidine in DNA and thus acts as an antimetabolite. It causes breaks in chromosomes and has been proposed as an antiviral and antineoplastic agent. It has been given orphan drug status for use in the treatment of primary brain tumors. BUdR,BrdU,Bromouracil Deoxyriboside,Broxuridine,5-Bromo-2'-deoxyuridine,5-Bromodeoxyuridine,NSC-38297,5 Bromo 2' deoxyuridine,5 Bromodeoxyuridine,Deoxyriboside, Bromouracil
D002478 Cells, Cultured Cells propagated in vitro in special media conducive to their growth. Cultured cells are used to study developmental, morphologic, metabolic, physiologic, and genetic processes, among others. Cultured Cells,Cell, Cultured,Cultured Cell
D000071163 Trefoil Factor-1 A 60 amino acid (6.5 kDa) trefoil factor that contains a single trefoil domain. It is expressed primarily by surface EPITHELIAL CELLS of the GASTRIC MUCOSA, where it associates with MUCIN 5AC. Protein pS2,TFF1 Peptide,TFF1 Protein,Trefoil Peptide 1,Trefoil Factor 1,pS2, Protein
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D001253 Astrocytes A class of large neuroglial (macroglial) cells in the central nervous system - the largest and most numerous neuroglial cells in the brain and spinal cord. Astrocytes (from "star" cells) are irregularly shaped with many long processes, including those with "end feet" which form the glial (limiting) membrane and directly and indirectly contribute to the BLOOD-BRAIN BARRIER. They regulate the extracellular ionic and chemical environment, and "reactive astrocytes" (along with MICROGLIA) respond to injury. Astroglia,Astroglia Cells,Astroglial Cells,Astrocyte,Astroglia Cell,Astroglial Cell,Astroglias,Cell, Astroglia,Cell, Astroglial

Related Publications

M Hirota, and S Miyashita, and H Hayashi, and Y Furukawa, and K Hayashi
June 1987, Experimental cell research,
M Hirota, and S Miyashita, and H Hayashi, and Y Furukawa, and K Hayashi
June 1994, Biochemistry and molecular biology international,
M Hirota, and S Miyashita, and H Hayashi, and Y Furukawa, and K Hayashi
September 1989, European journal of immunology,
M Hirota, and S Miyashita, and H Hayashi, and Y Furukawa, and K Hayashi
July 1978, Proceedings of the National Academy of Sciences of the United States of America,
M Hirota, and S Miyashita, and H Hayashi, and Y Furukawa, and K Hayashi
April 1991, Molecular and cellular biology,
M Hirota, and S Miyashita, and H Hayashi, and Y Furukawa, and K Hayashi
February 1991, Proceedings of the National Academy of Sciences of the United States of America,
M Hirota, and S Miyashita, and H Hayashi, and Y Furukawa, and K Hayashi
January 1991, Cold Spring Harbor symposia on quantitative biology,
M Hirota, and S Miyashita, and H Hayashi, and Y Furukawa, and K Hayashi
May 1997, Molecular and cellular biology,
M Hirota, and S Miyashita, and H Hayashi, and Y Furukawa, and K Hayashi
November 1989, Experimental cell research,
Copied contents to your clipboard!