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Helen Diller Family Compr Cancer Ctr
PRISCILLA K. COOPER, PHD

Senior Staff Scientist, Life Sciences Division, Lawrence Berkeley National Laboratory
Co-Leader, DNA Repair and Radiation Biology Program, UCSF Helen Diller Family Comprehensive Cancer Center

CONTACT

pkcooper@lbl.gov
(510) 486-7346 (voice)
(510) 486-6816 (fax)

Lawrence Berkeley Nat'l Lab; Mailstop 74-157
1 Cyclotron Road; Berkeley, CA 94720

additional websites:

Cooper Lab Website

EDUCATION

University of Rochester, Rochester, NY, B.A. (with high distinction), 1966, Biology
Stanford University, Stanford, CA, Ph.D., 1971, Biology
Stanford U. School of Medicine, Stanford, CA, Postdoc., 1971-1973, Genetics

PROFESSIONAL EXPERIENCE

1965, 1966

Summer Student, Biology Department, Brookhaven National Laboratory, Upton, L.I., NY

1966 -1968

Teaching Assistant, Department of Biological Sciences, Stanford University, Stanford, CA

1966 -1971

Graduate Student, Biological Sciences, Stanford University. Laboratory of P.C. Hanawalt.

1971 -1974

Postdoctoral Fellow, Genetics, Stanford Univ. School of Medicine. Lab of A.T. Ganesan.

1974 -1982

Research Associate, Dept. of Biological Sciences, Stanford University

1982 - 2000

Staff Scientist, Life Sciences Div., Lawrence Berkeley National Laboratory, Berkeley, CA

1984 -1987

Deputy Group Leader, Cell and Molecular Biology Group, BioMed Division (now Life Sciences), LBNL

1991 - present

Faculty Affiliate, Dept. Radiological Health Sciences Colorado State Univ., Ft. Collins CO

1995 - 1999

Deputy Head, Dept. of Radiation Biology & DNA Repair, Life Sciences Division, LBNL

1999 - present

Head, Dept. Cell & Molecular Biology (now Molecular Biology), Life Sciences Div., LBNL

2000 - present

Senior Scientist, Life Sciences Division, LBNL

2001 - 2003

Acting Division Director, Life Sciences Division, LBNL

HONORS & AWARDS

1962 - 1966

Bausch and Lomb Science Scholarship, University of Rochester

1966

Janet Howell Clarke Award (outstanding woman science graduate), Univ. of Rochester

1966

Phi Beta Kappa

1966

NSF Predoctoral Fellowship - 1970

1971 - 1973

NIH Postdoctoral Fellowship (NCI)

2002

Secretary of Energy Outstanding Mentor Award

SELECTED PUBLICATIONS

Cooper PK. Excision repair in mutants of E. coli deficient in DNA polymerase I and/or its associated 5' - 3' exonuclease. Mol. Gen. Genet. 150, 1-12 (1977).

Hanawalt PC, Cooper PK, Ganesan AK, and Smith CA. DNA repair in bacteria and mammalian cells. Ann. Rev. of Biochemistry 48, 783-836 (1979).

Cooper PK. Characterization of long patch excision repair of DNA in ultraviolet-irradiated Escherichia coli: an inducible function under Rec-Lex control. Mol. Gen. Genet. 185, 189-197 (1982).

Leadon SA and Cooper PK. Preferential repair of ionizing radiation-induced damage in the transcribed strand of an active human gene is defective in Cockayne Syndrome. Proc. Natl. Acad. Sci. 90, 10499-10503 (1993).

Rydberg B, Löbrich M, and Cooper PK. DNA double-strand breaks induced by high-energy Ne and Fe ions in human fibroblasts. I. Pulsed field gel electrophoresis method. Radiat. Res. 139, 133-141 (1994).

Löbrich M, Rydberg B, and Cooper PK. DNA double-strand breaks induced by high-energy Ne and Fe ions in human fibroblasts. II. Probing individual NotI fragments by hybridization. Radiat. Res. 139, 142-151 (1994).

Löbrich M, Rydberg B, and Cooper PK. Repair of X-ray-induced DNA double-strand breaks in specific NotI restriction fragments in human fibroblasts: joining of correct and incorrect ends. Proc. Natl. Acad. Sci. USA 92, 12050-12054 (1995).

Löbrich M, Rydberg B, and Cooper PK. Random-breakage mapping method applied to human DNA sequences. Nucleic Acids Res. 24, 1802-1809 (1996).

Löbrich M, Cooper PK, and Rydberg B. Non-random distribution of DNA double-strand breaks induced by particle irradiation. Internatl. J. Rad. Biol. 70, 493-503 (1996).

Cooper PK, Nouspikel T, Clarkson SG, and Leadon SA. Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G. Science 275, 990-993 (1997). Retracted: Science 308, 1740 (2005).

Nouspikel T, Lalle P, Leadon SA, Cooper PK, and Clarkson SG. A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: Implications for a second XPG function. Proc. Natl. Acad. Sci. USA 94, 3116-3121 (1997).

Löbrich M, Cooper PK, and Rydberg B. Joining of correct and incorrect DNA ends at double-strand breaks produced by high linear energy transfer radiation in human fibroblasts. Radiat. Res. 150, 619-626 (1998).

Fouladi B, Rydberg B, Waldren CA, and Cooper PK. Comparison of DNA double-strand break repair in identical sequences in primary human fibroblasts and immortal hamster-human hybrid cells harboring a normal human chromosome 11. Radiat. Res. 153, 795-804 (2000).

Le Page F, Kwoh EE, Avrutskaya A, Gentil A, Leadon SA, Sarasin A, and Cooper PK. Transcription-coupled base excision repair and mutation avoidance at 8-oxoguanine: Requirement for XPG, TFIIH, and CSB and implications for Cockayne syndrome. Cell 101, 159-171 (2000). Retracted: Cell 123, 711 (2005)

Weinfeld M, Xing JA, Lee J, Leadon SA, Cooper PK, and Le XC. Factors influencing the removal of thymine glycol from DNA in γ-irradiated human cells. Progr. Nucl. Acid Res. Mol. Biol. 68, 139-149 (2001).

Rydberg B, Heilbronn L, Holley W, Löbrich M, Zeitlin C, Chatterjee A, and Cooper PK. Spatial distribution and yield of DNA DSBs induced by 3-7 MeV helium ions in human fibroblasts. Radiat. Res.158, 32-42 (2002).

Wang J-Y, Sarker AH, Cooper PK, and Volkert MR. The single-strand DNA binding activity of human PC4 prevents mutagenesis and killing by oxidative DNA damage. Mol. Cell. Biol. 24, 6084-6093 (2004).

Rydberg B, Cooper B, Cooper PK, Holley WR, and Chatterjee A. Dose-Dependent Misrejoining of Radiation-Induced DNA Double-Strand Breaks in Human Fibroblasts: Experimental and Theoretical Study for High and Low LET Radiation. Radiat. Res. 163, 526-534 (2005).

Wang J, Pluth JM, Cooper PK, Cowan MJ, Chen DJ, and Yannone SM. Artemis Deficiency Confers a DNA Double-Strand Break Repair Defect and Artemis Phosphorylation Status is Altered by DNA Damage and Cell Cycle Progression. DNA Repair 4, 556-570 (2005).

Kalogeraki VS, Tornaletti S, Cooper PK, and Hanawalt PC. Comparative TFIIS-mediated transcript cleavage by mammalian RNA polymerase II arrested at a lesion in different transcription systems. DNA Repair 4, 1075-1087 (2005).

Sarker AH, Tsutakawa SE, Kostek S, Ng C, Shin DS, Peris M, Campeau E, Tainer JA, Nogales E, and Cooper PK. Recognition of RNA polymerase II and transcription bubbles by XPG, CSB, and TFIIH: Insights for transcription-coupled repair and Cockayne syndrome. Mol. Cell 20, 187-198 (2005).

Fan L, Arvai A, Cooper PK, Iwai S, Hanaoka F, Tainer JA. Conserved XPB core structure and motifs for DNA unwinding: Implications for pathway selection of transcription or excision repair. Mol. Cell 22, 27-37 (2006).

6/08/06

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