TY - JOUR
T1 - Intersections between transcription-coupled repair and alkylation damage reversal
AU - Brickner, Joshua R.
AU - Townley, Brittany A.
AU - Mosammaparast, Nima
N1 - Funding Information:
B.T. is supported by the Washington University Cell and Molecular Biology Training Grant (5T32GM007067-40). Work in the N.M. laboratory is supported by the NIH (R01 CA193318-05 and R01 CA227001-1), an American Cancer Society Research Scholar Grant, and the Siteman Cancer Center of Washington University.
Funding Information:
B.T. is supported by the Washington University Cell and Molecular Biology Training Grant ( 5T32GM007067-40 ). Work in the N.M. laboratory is supported by the NIH ( R01 CA193318-05 and R01 CA227001-1 ), an American Cancer Society Research Scholar Grant, and the Siteman Cancer Center of Washington University .
Publisher Copyright:
© 2019 Elsevier B.V.
PY - 2019/9
Y1 - 2019/9
N2 - The response to DNA damage intersects with many other physiological processes in the cell, such as DNA replication, chromatin remodeling, and the cell cycle. Certain damaging lesions, such as UV-induced pyrimidine dimers, also strongly block RNA polymerases, necessitating the coordination of the repair mechanism with remodeling of the elongating transcriptional machinery, in a process called transcription-coupled nucleotide excision repair (TC-NER). This pathway is typically not thought to be engaged with smaller lesions such as base alkylation. However, recent work has uncovered the potential for shared molecular components between the cellular response to alkylation and UV damage. Here, we review our current understanding of the alkylation damage response and its impacts on RNA biogenesis. We give particular attention to the Activating Signal Cointegrator Complex (ASCC), which plays important roles in the transcriptional response during UV damage as well as alkylation damage reversal, and intersects with trichothiodystrophy, an inherited disease associated with TC-NER.
AB - The response to DNA damage intersects with many other physiological processes in the cell, such as DNA replication, chromatin remodeling, and the cell cycle. Certain damaging lesions, such as UV-induced pyrimidine dimers, also strongly block RNA polymerases, necessitating the coordination of the repair mechanism with remodeling of the elongating transcriptional machinery, in a process called transcription-coupled nucleotide excision repair (TC-NER). This pathway is typically not thought to be engaged with smaller lesions such as base alkylation. However, recent work has uncovered the potential for shared molecular components between the cellular response to alkylation and UV damage. Here, we review our current understanding of the alkylation damage response and its impacts on RNA biogenesis. We give particular attention to the Activating Signal Cointegrator Complex (ASCC), which plays important roles in the transcriptional response during UV damage as well as alkylation damage reversal, and intersects with trichothiodystrophy, an inherited disease associated with TC-NER.
KW - ASCC
KW - AlkB
KW - Alkylation
KW - DNA damage
KW - Nucleotide excision repair
KW - RNF113A
KW - Transcription
KW - Trichothiodystrophy
UR - http://www.scopus.com/inward/record.url?scp=85069000004&partnerID=8YFLogxK
U2 - 10.1016/j.dnarep.2019.102663
DO - 10.1016/j.dnarep.2019.102663
M3 - Review article
C2 - 31326362
AN - SCOPUS:85069000004
SN - 1568-7864
VL - 81
JO - DNA Repair
JF - DNA Repair
M1 - 102663
ER -