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Metabolic formation of nucleoside-modified analogues of S-adenosylmethionine
Authors:T P Zimmerman  R D Deeprose  G Wolberg  G S Duncan
Affiliation:1. Department of Cell Biology Laboratory at Baylor College of Medicine, Houston, Texas, 77030 USA;2. Howard Hughes Medical Institute Laboratory at Baylor College of Medicine, Houston, Texas, 77030 USA
Abstract:A Pseudo-ovalbumin gene, bearing significant nucleotide sequence homology to the ovalbumin gene, has been cloned from genomic chick DNA. Similar to the authentic ovalbumin gene, the pseudo-gene is a unique sequence gene in the chick genome and is expressed at a low level in the immature chick oviduct. In contrast to the ovalbumin gene, expression of the pseudo-gene in the oviduct is not inducible by estrogen. The concentration of pseudo-gene RNA is only ~0.01% of that of authentic ovalbumin mRNA in estrogen-stimulated oviduct cells. Nucleotide sequence analysis of the two sequence related genes may reveal the molecular basis of differential response to steroid hormone induction in the same tissue.
Keywords:AdoMet  S-adenosylmethionine  AdoHcy  S-adenosylhomocysteine  7-deazaadenosine  S-7-deazaadenosylmethionine  COMT  catechol-O-methyltransferase (EC 2.1.1.6)  3′-dAdo  3′-deoxyadenosine  3′-dAdoMet  S-3′-deoxyadenosylmethionine  EHNA  FAdo  2-fluoroadenosine  FAdoMet  S-2-fluoroadenosylmethionine  For  formycin A  ForMet  S-formycinylmethionine  HPLC  high-performance liquid chromatography  Neb  nebularine  NebMet  S-nebularylmethionine  8-azaadenosine  S-8-azaadenosylmethionine
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