Rpb9-deficient cells are defective in DNA damage response and require histone H3 acetylation for survival.

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Rpb9-deficient cells are defective in DNA damage response and require histone H3 acetylation for survival.

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2018 nî lūn-bûn

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Rpb9-deficient cells are defec ...... e H3 acetylation for survival.

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Rpb9-deficient cells are defec ...... e H3 acetylation for survival.

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Rpb9-deficient cells are defec ...... e H3 acetylation for survival.

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Rpb9-deficient cells are defec ...... e H3 acetylation for survival.

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Rpb9-deficient cells are defec ...... e H3 acetylation for survival.

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Rpb9-deficient cells are defec ...... e H3 acetylation for survival.

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P1476

Rpb9-deficient cells are defec ...... ne H3 acetylation for survival

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Henel Sein

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Kadri Peil

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Kersti Kristjuhan

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Kristina Reinmets

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Signe Värv

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P2860

Structure and ligand of a histone acetyltransferase bromodomain

Histone H3 lysine 56 acetylation and the response to DNA replication fork damage

Rad52 forms DNA repair and recombination centers during S phase.

Evidence that the transcription elongation function of Rpb9 is involved in transcription-coupled DNA repair in Saccharomyces cerevisiae.

Transcription elongation through DNA arrest sites. A multistep process involving both RNA polymerase II subunit RPB9 and TFIIS.

Rad9 BRCT domain interaction with phosphorylated H2AX regulates the G1 checkpoint in budding yeast.

A role for Saccharomyces cerevisiae histone H2A in DNA repair.

Binding of chromatin-modifying activities to phosphorylated histone H2A at DNA damage sites.

Bre1, an E3 ubiquitin ligase required for recruitment and substrate selection of Rad6 at a promoter.

RNA polymerase II subunit Rpb9 is important for transcriptional fidelity in vivo

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2949

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scholarly article

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10.1038/S41598-018-21110-9

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English

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Arnold Kristjuhan

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2018-02-13T00:00:00Z

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29440683

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5811553

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