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	<title>Telomeric repeat-binding factor 2 - Revision history</title>
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		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;== Telomeric Repeat-binding Factor 2 ==&lt;br /&gt;
&lt;br /&gt;
[[File:TERF2_Domains.png|thumb|right|Diagram of TERF2 domains]]&lt;br /&gt;
&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;Telomeric repeat-binding factor 2&amp;#039;&amp;#039;&amp;#039; (TERF2) is a crucial protein involved in the maintenance and protection of [[telomeres]], the specialized structures at the ends of [[chromosomes]]. TERF2 is part of the shelterin complex, a group of proteins that specifically bind to telomeric DNA and regulate its structure and function.&lt;br /&gt;
&lt;br /&gt;
== Structure ==&lt;br /&gt;
&lt;br /&gt;
TERF2 is characterized by several distinct domains that contribute to its function. The protein contains a [[Myb domain]], which is responsible for binding to the telomeric DNA sequence. Additionally, TERF2 has a TRFH (TERF2 homology) domain that mediates protein-protein interactions, allowing it to recruit other components of the shelterin complex.&lt;br /&gt;
&lt;br /&gt;
== Function ==&lt;br /&gt;
&lt;br /&gt;
The primary role of TERF2 is to protect telomeres from being recognized as sites of DNA damage. It achieves this by facilitating the formation of a T-loop structure, where the single-stranded 3&amp;#039; overhang of the telomere invades the double-stranded region, effectively hiding the chromosome end. This structure prevents the activation of DNA damage response pathways that would otherwise lead to inappropriate repair activities.&lt;br /&gt;
&lt;br /&gt;
TERF2 also plays a role in the recruitment of other proteins to the telomere. It interacts with various client proteins that are involved in telomere maintenance and DNA repair processes.&lt;br /&gt;
&lt;br /&gt;
[[File:TERF2_client_protein_recruitment.png|thumb|left|TERF2 recruitment of client proteins]]&lt;br /&gt;
&lt;br /&gt;
== Role in Telomere Maintenance ==&lt;br /&gt;
&lt;br /&gt;
TERF2 is essential for the stability and integrity of telomeres. By maintaining the T-loop structure, TERF2 prevents the activation of [[ATM]] and [[ATR]] kinase pathways, which are typically triggered by DNA double-strand breaks. This protective function is crucial for preventing [[chromosomal instability]] and [[genomic instability]], which can lead to [[cancer]] and other age-related diseases.&lt;br /&gt;
&lt;br /&gt;
== Clinical Significance ==&lt;br /&gt;
&lt;br /&gt;
Dysfunction of TERF2, whether through mutation or altered expression, can lead to telomere shortening and genomic instability. This has been implicated in various diseases, including [[cancer]] and [[premature aging syndromes]]. Understanding the precise mechanisms by which TERF2 operates is therefore of great interest in the field of [[oncology]] and [[gerontology]].&lt;br /&gt;
&lt;br /&gt;
== Related Pages ==&lt;br /&gt;
&lt;br /&gt;
* [[Telomere]]&lt;br /&gt;
* [[Shelterin]]&lt;br /&gt;
* [[DNA damage response]]&lt;br /&gt;
* [[Chromosome]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Telomere biology]]&lt;br /&gt;
[[Category:DNA-binding proteins]]&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
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