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4J19

Structure of a novel telomere repeat binding protein bound to DNA

Summary for 4J19
Entry DOI10.2210/pdb4j19/pdb
DescriptorHomeobox-containing protein 1, DNA (5'-D(*CP*TP*GP*TP*TP*AP*GP*GP*GP*TP*TP*AP*GP*GP*GP*TP*TP*AP*G)-3'), DNA (5'-D(*TP*CP*TP*AP*AP*CP*CP*CP*TP*AP*AP*CP*CP*CP*TP*AP*AP*CP*A)-3'), ... (5 entities in total)
Functional Keywordstelomere repeat binding, telomeric dna, transcription-dna complex, transcription/dna
Biological sourceHomo sapiens (human)
Cellular locationNucleus . Isoform 5: Nucleus : Q6NT76
Total number of polymer chains4
Total formula weight37865.87
Authors
Primary citationKappei, D.,Butter, F.,Benda, C.,Scheibe, M.,Draskovic, I.,Stevense, M.,Novo, C.L.,Basquin, C.,Araki, M.,Araki, K.,Krastev, D.B.,Kittler, R.,Jessberger, R.,Londono-Vallejo, J.A.,Mann, M.,Buchholz, F.
HOT1 is a mammalian direct telomere repeat-binding protein contributing to telomerase recruitment.
Embo J., 32:1681-1701, 2013
Cited by
PubMed Abstract: Telomeres are repetitive DNA structures that, together with the shelterin and the CST complex, protect the ends of chromosomes. Telomere shortening is mitigated in stem and cancer cells through the de novo addition of telomeric repeats by telomerase. Telomere elongation requires the delivery of the telomerase complex to telomeres through a not yet fully understood mechanism. Factors promoting telomerase-telomere interaction are expected to directly bind telomeres and physically interact with the telomerase complex. In search for such a factor we carried out a SILAC-based DNA-protein interaction screen and identified HMBOX1, hereafter referred to as homeobox telomere-binding protein 1 (HOT1). HOT1 directly and specifically binds double-stranded telomere repeats, with the in vivo association correlating with binding to actively processed telomeres. Depletion and overexpression experiments classify HOT1 as a positive regulator of telomere length. Furthermore, immunoprecipitation and cell fractionation analyses show that HOT1 associates with the active telomerase complex and promotes chromatin association of telomerase. Collectively, these findings suggest that HOT1 supports telomerase-dependent telomere elongation.
PubMed: 23685356
DOI: 10.1038/emboj.2013.105
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.9 Å)
Structure validation

237735

数据于2025-06-18公开中

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