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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=ARIH2</id>
	<title>ARIH2 - История изменений</title>
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	<updated>2026-06-12T11:15:35Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=ARIH2&amp;diff=5918&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «E3 ubiquitin-protein ligase ARIH2 (EC 2.3.2.31) (ARI-2) (Protein ariadne-2 homolog) (RING-type E3 ubiquitin transferase ARIH2) (Triad1 protein) [ARI2] [TRIAD1] [H...»</title>
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		<updated>2021-05-12T15:00:12Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «E3 ubiquitin-protein ligase ARIH2 (EC 2.3.2.31) (ARI-2) (Protein ariadne-2 homolog) (RING-type E3 ubiquitin transferase ARIH2) (Triad1 protein) [ARI2] [TRIAD1] [H...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;E3 ubiquitin-protein ligase ARIH2 (EC 2.3.2.31) (ARI-2) (Protein ariadne-2 homolog) (RING-type E3 ubiquitin transferase ARIH2) (Triad1 protein) [ARI2] [TRIAD1] [HT005]&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=A novel feed-forward loop between [[ARIH2]] E3-ligase and [[PABPN1]] regulates aging-associated muscle degeneration.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/24486325&lt;br /&gt;
|abstract=Alanine expansion mutations in poly(A)-binding protein nuclear 1 ([[PABPN1]]) cause muscle weakness in the late-onset disorder oculopharyngeal muscular dystrophy. In affected muscles, expanded [[PABPN1]] forms nuclear aggregates, depleting levels of soluble [[PABPN1]] and inducing a genome-wide shift from distal to proximal polyadenylation site usage. [[PABPN1]] protein accumulation is regulated by the ubiquitin proteasome system, which is highly dysregulated in oculopharyngeal muscular dystrophy. We show that [[ARIH2]] E3-ligase regulates [[PABPN1]] protein accumulation and aggregation. Levels of [[ARIH2]] mRNA are regulated by [[PABPN1]] via proximal polyadenylation site usage. We demonstrate that masking the proximal polyadenylation site in [[ARIH2]] 3&amp;#039; untranslated region by antisense oligonucleotides elevates the expression of [[ARIH2]] and [[PABPN1]] and restores myogenic defects that are induced by [[ARIH2]] or [[PABPN1]] down-regulation in cell culture. In vivo [[ARIH2]] mRNA levels significantly decrease from midlife in vastus lateralis muscles and highly correlate with muscle degeneration. We suggest that the expression of both genes is maintained by a feed-forward loop between mRNA stability regulated by [[PABPN1]] and protein turnover regulated by [[ARIH2]]. &lt;br /&gt;
|mesh-terms=* Aging&lt;br /&gt;
* Animals&lt;br /&gt;
* Blotting, Western&lt;br /&gt;
* Cell Line&lt;br /&gt;
* Gene Expression Regulation&lt;br /&gt;
* Humans&lt;br /&gt;
* Immunohistochemistry&lt;br /&gt;
* Immunoprecipitation&lt;br /&gt;
* Muscle, Skeletal&lt;br /&gt;
* Muscular Dystrophy, Oculopharyngeal&lt;br /&gt;
* Oligonucleotide Array Sequence Analysis&lt;br /&gt;
* Poly(A)-Binding Protein I&lt;br /&gt;
* Reverse Transcriptase Polymerase Chain Reaction&lt;br /&gt;
* Transfection&lt;br /&gt;
* Ubiquitin-Protein Ligases&lt;br /&gt;
&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1016/j.ajpath.2013.12.011&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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