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Telomere C-Strand Fill-In Machinery: New Insights into the Human CST-DNA Polymerase Alpha-Primase Structures and Functions.
Lim, Ci Ji.
Affiliation
  • Lim CJ; Department of Biochemistry, College of Agricultural and Life Sciences, University of Wisconsin-Madison, Madison, WI, USA. ciji.lim@wisc.edu.
Subcell Biochem ; 104: 73-100, 2024.
Article de En | MEDLINE | ID: mdl-38963484
ABSTRACT
Telomeres at the end of eukaryotic chromosomes are extended by a specialized set of enzymes and telomere-associated proteins, collectively termed here the telomere "replisome." The telomere replisome acts on a unique replicon at each chromosomal end of the telomeres, the 3' DNA overhang. This telomere replication process is distinct from the replisome mechanism deployed to duplicate the human genome. The G-rich overhang is first extended before the complementary C-strand is filled in. This overhang is extended by telomerase, a specialized ribonucleoprotein and reverse transcriptase. The overhang extension process is terminated when telomerase is displaced by CTC1-STN1-TEN1 (CST), a single-stranded DNA-binding protein complex. CST then recruits DNA polymerase α-primase to complete the telomere replication process by filling in the complementary C-strand. In this chapter, the recent structure-function insights into the human telomere C-strand fill-in machinery (DNA polymerase α-primase and CST) will be discussed.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Télomère / DNA primase / Protéines télomériques / DNA polymerase I / Réplication de l'ADN Limites: Humans Langue: En Journal: Subcell Biochem Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Télomère / DNA primase / Protéines télomériques / DNA polymerase I / Réplication de l'ADN Limites: Humans Langue: En Journal: Subcell Biochem Année: 2024 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: États-Unis d'Amérique