Angular distributions of C 1s photoelectrons, relative to a dissociation axis for C2H2, have been measured with a photoelectron–photoion–photoion coincidence technique. The photoelectron angular distribution (PAD) for three two-body fragmentations (symmetric, non-symmetric and proton-migration fragmentations) is completely different. The PADs for non-symmetric fragmentation provide direct evidence of a localized core-hole and preferential bond breaking following Auger decays. Moreover, the PAD for symmetric fragmentation has been interpreted as the interference between photoemissions from the two carbon atoms.
Summary We previously isolated two distinct Saccharomyces cerevisiae myo ‐inositol transporter genes, ITR1 and ITR2 (Nikawa et al. , 1991). Here, we studied the regulation of their expression by measuring steady‐state mRNA levels and β‐galactosidase activities of lacZ fusion genes under different conditions. The results show that the expression of the two ITR genes is differently regulated: ITR1 was repressed by inositol and choline whereas ITR2 was constitutive. Deletion analysis of the ITR1 upstream region and comparison with the upstream regions of other genes involved in phospholipid synthesis indicate that the octamer sequence 5′‐TTCACATG‐3′ is important for the expression and inositol/choline regulation of the ITR1 gene.
The regulation of choline kinase (EC 2.7.1.32), the initial enzyme in the CDP-choline pathway, was examined in Saccharomyces cerevisiae. The addition of myo-inositol to a culture of wild-type cells resulted in a significant decrease in choline kinase activity. Additional supplementation of choline caused a further reduction in the activity. The coding frame of the choline kinase gene, CK1, was joined to the carboxyl terminus of lacZ and expressed in Escherichia coli as a fusion protein, which was then used to prepare an anti-choline kinase antibody. Upon Western (immuno-) and Northern (RNA) blot analyses using the antibody and a CK1 probe, respectively, the decrease in the enzyme activity was found to be correlated with decreases in the enzyme amount and mRNA abundance. The molecular mass of the enzyme was estimated to be 66 kilodaltons, in agreement with the value predicted previously from the nucleotide sequence of the gene. The coding region of CK1 was replaced with that of lacZ, and CK1 expression was measured by assaying beta-galactosidase. The expression of beta-galactosidase from this fusion was repressed by myo-inositol and choline and derepressed in a time-dependent manner upon their removal. The present findings indicate that yeast choline kinase is regulated by myo-inositol and choline at the level of mRNA abundance.
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