TY - JOUR
T1 - Requirement for yeast RAD26, a homolog of the human CSB gene, in elongation by RNA polymerase II
AU - Lee, S. K.
AU - Yu, S. L.
AU - Prakash, L.
AU - Prakash, S.
PY - 2001
Y1 - 2001
N2 - Mutations in the human CSB gene cause Cockayne syndrome (CS). In addition to increased photosensitivity, CS patients suffer from severe developmental abnormalities, including growth retardation and mental retardation. Whereas a deficiency in the preferential repair of UV lesions from the transcribed strand accounts for the increased photosensitivity of CS patients, the reason for developmental defects in these individuals has remained unclear. Here we provide in vivo evidence for a role of RAD26, the counterpart of the CSB gene in Sacharomyces cerevisiae, in transcription elongation by RNA polymerase II, and in addition we show that under conditions requiring rapid synthesis of new mRNAs, growth is considerably reduced in cells lacking RAD26. These findings implicate a role for CSB in transcription elongation, and they strongly suggest that impaired transcription elongation is the underlying cause of the developmental problems in CS patients.
AB - Mutations in the human CSB gene cause Cockayne syndrome (CS). In addition to increased photosensitivity, CS patients suffer from severe developmental abnormalities, including growth retardation and mental retardation. Whereas a deficiency in the preferential repair of UV lesions from the transcribed strand accounts for the increased photosensitivity of CS patients, the reason for developmental defects in these individuals has remained unclear. Here we provide in vivo evidence for a role of RAD26, the counterpart of the CSB gene in Sacharomyces cerevisiae, in transcription elongation by RNA polymerase II, and in addition we show that under conditions requiring rapid synthesis of new mRNAs, growth is considerably reduced in cells lacking RAD26. These findings implicate a role for CSB in transcription elongation, and they strongly suggest that impaired transcription elongation is the underlying cause of the developmental problems in CS patients.
UR - http://www.scopus.com/inward/record.url?scp=0035201056&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0035201056&partnerID=8YFLogxK
U2 - 10.1128/MCB.21.24.8651-8656.2001
DO - 10.1128/MCB.21.24.8651-8656.2001
M3 - Article
C2 - 11713297
AN - SCOPUS:0035201056
SN - 0270-7306
VL - 21
SP - 8651
EP - 8656
JO - Molecular and cellular biology
JF - Molecular and cellular biology
IS - 24
ER -