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Glucosylated hydroxymethyluracil, DNA base J, prevents transcriptional readthrough in Leishmania.

Henri G A M van Luenen ,
Carol Farris ,
Sabrina Jan ,
Paul-Andre Genest ,
Pankaj Tripathi ,
Arno Velds ,
Ron M Kerkhoven ,
Marja Nieuwland ,
Andrew Haydock ,
Gowthaman Ramasamy ,
Saara Vainio ,
Tatjana Heidebrecht ,
Anastassis Perrakis ,
Ludo Pagie ,
Bas van Steensel ,
Peter J Myler ,
Piet Borst

Abstract

Some Ts in nuclear DNA of trypanosomes and Leishmania are hydroxylated and glucosylated to yield base J (β-D-glucosyl-hydroxymethyluracil). In Leishmania, about 99% of J is located in telomeric repeats. We show here that most of the remaining J is located at chromosome-internal RNA polymerase II termination sites. This internal J and telomeric J can be reduced by a knockout of J-binding protein 2 (JBP2), an enzyme involved in the first step of J biosynthesis. J levels are further reduced by growing Leishmania JBP2 knockout cells in BrdU-containing medium, resulting in cell death. The loss of internal J in JBP2 knockout cells is accompanied by massive readthrough at RNA polymerase II termination sites. The readthrough varies between transcription units but may extend over 100 kb. We conclude that J is required for proper transcription termination and infer that the absence of internal J kills Leishmania by massive readthrough of transcriptional stops.

More about this publication

Cell

Volume 150
Issue nr. 5
Pages 909-21
Publication date 31-08-2012

Full text links

Publisher website (DOI) 10.1016/j.cell.2012.07.030
Europe PubMed Central 22939620
Pubmed 22939620

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