Search PubMed⌕ Search

PubMed · 2861819

Decrease in tyrosine hydroxylase synthesis in cultured adrenal medulla by N6-methyladenosine.

Abstract

Explants of adrenal medullae were cultured in defined media for up to 22 hr, during which time the tissue remained histologically intact. Addition of N6-methyladenosine to the medium led to a diminution in the activity of tyrosine hydroxylase (EC 1.14.16.2) in the tissue. The enzyme activity was inversely proportional to the concentration of N6-methyladenosine in the culture medium. The extent of loss of tyrosine hydroxylase, as measured by immunochemical titration, corresponded to the degree of loss in enzyme activity under the same conditions. The decreased amount of enzyme protein was due to a decreased rate of synthesis of tyrosine hydroxylase. A significant decrease in the relative rate of tyrosine hydroxylase synthesis indicates the selectivity of this effect of N6-methyladenosine. The rate of enzyme degradation was not affected by this compound. Neither adenosine, N6-cyclohexyladenosine, nor several other methylated nucleosides including N1-methyladenosine, N7-methylguanosine and N2-methylguanosine had an effect on the enzyme. However, two other N6-substituted adenosines, N6-dimethyladenosine and N6-gamma gamma-dimethylallyladenosine, were effective in reducing tyrosine hydroxylase. The results are consistent with the view that specific substitutions at the N6 position of adenosine could play a role in regulation of levels of tyrosine hydroxylase by altering its rate of biosynthesis.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

W J Burke, T H Joh. 1985-08-01. Decrease in tyrosine hydroxylase synthesis in cultured adrenal medulla by N6-methyladenosine.. https://doi.org/10.1016/0006-2952(85)90558-1

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Solution structure of domain 6 from a self-splicing group II intron ribozyme: a Mg(2+) binding site is located close to the stacked branch adenosine.

Group II intron self-splicing is essential for the correct expression of organellar genes in plants, fungi, and yeast, as well as of bacterial genes. Self-excision of these autocatalytic introns from the primary RNA transcript is achieved in a two-step mechanism that is apparently analogous to that of the eukaryotic spliceosome. The 2'-OH of a conserved adenosine (the branch point) located within domain 6 (D6) acts as the nucleophile in the first step of splicing. Despite the biological importance of group II introns, little is known about their structural organization and usage of metal ions in catalysis. Here we report the first solution structure of a catalytically active D6 construct encompassing the branch point and the neighboring helical regions from the mitochondrial yeast intron ai5gamma. The branch adenosine is the single unpaired nucleotide, and, in contrast to the spliceosomal branch site, resides within the helix, being partially stacked between two flanking GU wobble pairs. We identified a novel prominent Mg(2+) binding site in the major groove of the branch site. Importantly, Mg(2+) addition does not impair the stacking of the branch adenosine, rather it strengthens the interaction with the flanking uridines, as shown by NMR and fluorescence studies. This means that domain 6 presents the branch adenosine in a stacked fashion to the core of group II introns upon folding to the active conformation.

Adenosine↗

Synthesis and biological evaluation of novel 1-deoxy-1-[6-[((hetero)arylcarbonyl)hydrazino]- 9H-purin-9-yl]-N-ethyl-beta-D-ribofuranuronamide derivatives as useful templates for the development of A2B adenosine receptor agonists.

The lack of molecules endowed with selective and potent agonistic activity toward the hA2B adenosine receptors has limited the studies on this pharmacological target and consequently the evaluation of its therapeutic potential. We report the design and the synthesis of the first potent (EC50 in the nanomolar range) and selective hA2B adenosine receptor agonists consisting of 1-deoxy-1-[6-[((hetero)arylcarbonyl)hydrazino]-9H-purin-9-yl]-N-ethyl-beta-D-ribofuranuronamide derivatives. The concurrent effect of 6-substitution of the purine nucleus with a ((hetero)arylcarbonyl)hydrazino function and a 2-chloro substitution has been investigated in such NECA derivatives.

Adenosine↗

Enhanced CXCL1 production and angiogenesis in adenosine-mediated lung disease.

Angiogenesis is a feature of chronic lung diseases such as asthma and pulmonary fibrosis; however, the pathways controlling pathological angiogenesis during lung disease are not completely understood. Adenosine is a signaling molecule that has been implicated in the exacerbation of chronic lung disease and in the regulation of angiogenesis; however, the relationship between these factors has not been investigated. The current study utilized adenosine deaminase (ADA)-deficient mice to determine whether chronic elevations in adenosine in vivo result in pulmonary angiogenesis. Results demonstrate substantial angiogenesis in the tracheas of ADA-deficient mice in association with adenosine elevations. ADA replacement enzyme therapy resulted in a lowering of adenosine levels and reversal of tracheal angiogenesis, indicating that the increases in vessel number are dependent on adenosine elevations. Levels of the angiogenic chemokine CXCL1 (mouse functional homologue of human IL-8) were found to be elevated in an adenosine-dependent manner in the lungs of ADA-deficient mice. Neutralization of CXCL1 and its receptor, CXCR2, resulted in the inhibition of angiogenic activity, which suggests that CXCL1 signaling through the CXCR2 receptor mediated the observed increases in angiogenesis. Our findings suggest that adenosine plays an important role, via CXCL1, in the induction of pulmonary angiogenesis.

Adenosine↗