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Hiroshi Tauchi Eigo Matsumoto Kenta Iijima Daisuke Mochizuki Kenshi Komatsu Yusuke Ichimasa 《Biological Sciences in Space》2003,17(3):255-256
DNA double strand break (DSB) causes many cytotoxic effects such as cellular lethality, somatic mutation, and carcinogenesis. Fidelity of DSB repair is a important factor that determines the quality of genomic stability. It is known that the most of DSBs are properly repaired on the earth, however, little is known whether those are rejoined at the same fidelity even under the space environment. One of the DSB repair pathway, homologous recombination (HR), allows the cells to repair their DSBs with error free. Therefore, the efficiency of HR is a good index to assess the fidelity of DSB repair. In order to clarify the effect of gravity stress on HR pathway, we established a cell line that can detect a site-specific DNA repair via HR. The cells carrying a reporter construct for HR were incubated under hypergravity condition after induction of site specific DSB. Our preliminary results suggest that the gravity stress may affect the HR efficiency. 相似文献
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Occurrence of a factor(s) which can selectively inhibit ribosomal RNA synthesis in isolated neurula cells of Xenopus laevis was examined in oocytes, unfertilized eggs, and embryos of Xenopus laevis. It was found that acid-soluble materials from full-sized oocytes, white-banded mature oocytes, unfertilized eggs, and pregastrular embryos were all active in significantly reducing the relative ratio of the [3H]uridine incorporation into 18S and 28S ribosomal RNA to that into 4S RNA from the control value. These results suggest that the inhibitor appears in the terminal step of oogenesis and, hence, may be assumed as a maternal regulator. 相似文献
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H Shimoi T Kawahara K Suzuki Y Iwasaki A Y Jeng Y Nishikawa 《European journal of biochemistry》1992,209(1):189-194
The C-terminal amide structure of peptide hormones and neurotransmitters is synthesized via a two-step reaction catalyzed by peptidylglycine alpha-hydroxylating monooxygenase (PHM) and peptidylhydroxyglycine N-C lyase. A Xenopus laevis PHM expressed in insect-cell culture by the baculovirus-expression-vector system was purified to homogeneity and characterized. Using a newly established assay system for PHM, the kinetic features of this enzyme were investigated. As expected, the enzyme required copper ions, L-ascorbate and molecular oxygen for turnover. Salts like KI and KCl, and catalase stabilized the enzyme in the presence of L-ascorbate. The optimum pH value for the enzyme reaction was around six when Mes buffer was used and around seven when phosphate buffer was used under the same assay condition. Below pH 6, acetate, iodide and chloride ions activated the reaction. The kinetic analysis is consistent with a ping-pong mechanism with respect to peptide and L-ascorbate, and the peptide showed substrate inhibition. The substrate specificity of the enzyme at the penultimate position was examined by competitive assay using tripeptides with glycine at the C-termini and the inhibitory potency of these peptides in descending order was methionine > aromatic > non-polar amino acids. 相似文献
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Mechanisms of somatic embryogenesis in cell cultures: Physiology,biochemistry, and molecular biology
A. Komamine R. Kawahara M. Matsumoto S. Sunabori T. Toya A. Fujiwara M. Tsukahara J. Smith M. Ito H. Fukuda K. Nomura T. Fujimura 《In vitro cellular & developmental biology. Plant》1992,28(1):11-14
Summary One of the most characteristic cell functions in plants is totipotency. Somatic embryogenesis can be regarded as a model system
for the investigation of mechanisms of totipotency, because a high frequency and synchronous embryogenic system from single
somatic cells has been established in carrot suspension cultures. Four phases are recognized in this process, and several
molecular markers, viz. polypeptides, mRNAs, antigens against monoclonal antibodies, can be detected during the expression
of totipotency, but they disappear during its loss. Four organ-specific genes have been isolated from hypocotyls and roots
by differential screening. They were expressed preferentially after the globular-heart stages of embryogenesis, and were strongly
suppressed by auxin. A CEM 1 gene was isolated by differential screening of embryogenic cell clusters. This gene was expressed
strongly and transiently during the proglobular and globular stages. The sequence of CEM 1 was found to encode a polypeptide
showing high homology to the elongation factor isolated from eucaryotic cells. Thus good progress is being made in understanding
the basic mechanisms of somatic embryogenesis.
Presented in the Session-in-Depth Developmental Biology of Embryogenesis at the 1991 World Congress on Cell and Tissue Culture,
Anaheim, California, June 16–20, 1991. 相似文献