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	<id>https://transhumanist.ru/index.php?action=history&amp;feed=atom&amp;title=MCM6</id>
	<title>MCM6 - История изменений</title>
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	<updated>2026-06-20T13:14:57Z</updated>
	<subtitle>История изменений этой страницы в вики</subtitle>
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		<id>https://transhumanist.ru/index.php?title=MCM6&amp;diff=4396&amp;oldid=prev</id>
		<title>OdysseusBot: Новая страница: «DNA replication licensing factor MCM6 (EC 3.6.4.12) (p105MCM)  ==Publications==  {{medline-entry |title=Changes in MCM2-7 proteins at senescence. |pubmed-url=...»</title>
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		<updated>2021-04-29T19:16:00Z</updated>

		<summary type="html">&lt;p&gt;Новая страница: «DNA replication licensing factor MCM6 (EC 3.6.4.12) (p105MCM)  ==Publications==  {{medline-entry |title=Changes in &lt;a href=&quot;/MCM2&quot; title=&quot;MCM2&quot;&gt;MCM2&lt;/a&gt;-7 proteins at senescence. |pubmed-url=...»&lt;/p&gt;
&lt;p&gt;&lt;b&gt;Новая страница&lt;/b&gt;&lt;/p&gt;&lt;div&gt;DNA replication licensing factor MCM6 (EC 3.6.4.12) (p105MCM)&lt;br /&gt;
&lt;br /&gt;
==Publications==&lt;br /&gt;
&lt;br /&gt;
{{medline-entry&lt;br /&gt;
|title=Changes in [[MCM2]]-7 proteins at senescence.&lt;br /&gt;
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/31092751&lt;br /&gt;
|abstract=Cellular aging is characterized by the loss of DNA replication capability and is mainly brought about by various changes in chromatin structure. Here, we examined changes in [[MCM2]]-7 proteins, which act as a replicative DNA helicase, during aging of human WI38 fibroblasts at the single-cell level. We used nuclear accumulation of p21 as a marker of senescent cells, and examined changes in [[MCM2]]-7 by western blot analysis. First, we found that senescent cells are enriched for cells with a DNA content higher than 4N. Second, the levels of [[MCM2]], [[MCM3]], [[MCM4]] and [[MCM6]] proteins decreased in senescent cells. Third, cytoplasmic localization of [[MCM2]] and [[MCM7]] was observed in senescent cells, from an analysis of [[MCM2]]-7 except for [[MCM5]]. Consistent with this finding, fragmented [[MCM2]] was predominant in these cells. These age-dependent changes in [[MCM2]]-7, a protein complex that directly affects cellular DNA replication, may play a critical role in cellular senescence.&lt;br /&gt;
|mesh-terms=* Cell Cycle Proteins&lt;br /&gt;
* Cellular Senescence&lt;br /&gt;
* DNA Replication&lt;br /&gt;
* Gene Expression Regulation&lt;br /&gt;
* Humans&lt;br /&gt;
* Minichromosome Maintenance Complex Component 2&lt;br /&gt;
* Minichromosome Maintenance Complex Component 3&lt;br /&gt;
* Minichromosome Maintenance Complex Component 4&lt;br /&gt;
* Minichromosome Maintenance Complex Component 6&lt;br /&gt;
* Minichromosome Maintenance Complex Component 7&lt;br /&gt;
* Multiprotein Complexes&lt;br /&gt;
* Single-Cell Analysis&lt;br /&gt;
* p21-Activated Kinases&lt;br /&gt;
|keywords=* DNA content&lt;br /&gt;
* MCM2–7 proteins&lt;br /&gt;
* cellular aging&lt;br /&gt;
* cellular localization&lt;br /&gt;
* protein degradation&lt;br /&gt;
|full-text-url=https://sci-hub.do/10.1266/ggs.18-00062&lt;br /&gt;
}}&lt;/div&gt;</summary>
		<author><name>OdysseusBot</name></author>
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