Office: SRTC 2107
Phone: 405-325-4912
Email: broe@ou.edu
Group Homepage
Link
Full
Publications List and Vitae
|
Bruce A. Roe
- George Lynn Cross Research Professor.
- B.A. (Hope College) 1963
- M.A., Ph.D. (Western Michigan) 1967, 1970.
- NIH Postdoctoral Fellow (SUNY at Stony Brook)
1970-1973
- NIH Research Career Development Award, 1976-1981
- Regents' Award for Superior Accomplishment
in Research, 1984
- George Lynn Cross Research Professor, 1997
|
Division:
Research Interests
- Nucleic acid structure and function;cloning,
sequence, and expression of mammalian mitochondrial
and cytoplasmic tRNAs; mammalian protein synthesis;
alterations in tRNA structure during normal
and abnormal cellular development; modified
nucleotides in mammalian tRNAS.
|
Research Description
Our laboratory presently is one of the NIH designated
Centers involved in the Human Genome Project, whose
goal is to determine the complete sequence of the 3
Billion base paired human chromosomes by 2005. During
the past decade we have played a major role in developing
many of the techniques needed to complete this goal,
as well as trained many of the MS and PhD scientists
actively involved in this project worldwide, and implementing
new robotics and computer based analysis methods. We
also are sequencing several bacterial genomes and actively
discovering the new and unique genes in both humans
and bacteria. These studies have and will continue to
provide an in-depth genetic based understanding of normal
gene function and the alterations that occur in a myriad
of genetic-based diseases.
Come visit us at the Chromosome
22 site where you will find lots of detail about
our work and the people in the lab.
Selected Recent Publications
R. H. Waterston, K. Lindblad-Toh, E. Birney, J. Rogers,
et al. Initial sequencing and comparative analysis of
the mouse genome. Nature 420, 520 - 562 (2002).
D. Ajdic, W. M. McShan, R. E. McLaughlin, G. Savic, J.
Chang, M. B. Carson, C. Primeaux, R. Tian, S. Kenton,
H. Jia, S. Lin, Y. Qian, S., Li, H. Zhu, F. Najar, H.
Lai, J. White, Genome sequence of Streptococcus mutans
UA159, a cariogenic dental pathogen. B. A. Roe, and J.
J., Ferretti. Proceeding National Academy Science 99,
14434-14439 (2002).
J. Kone, J. Arroyo, T. Savinelli, S. Lin, K. Boyd, Y.
Wu, M. Nimmakayalu, N.G. Copeland, N.A. Jenkins, M. Qumsiyeh,
P. Hu, A. Prescott,, H. Wu, L. Yang L, B.A. Roe and A.S.
Perkins. F-MuLV acceleration of myelomonocytic tumorigenesis
in SV40 large T antigen transgenic mice is accompanied
by retroviral insertion at Fli1 and a novel locus, Fim4.
Leukemia 16(9):1827-34 (2002)
K. Sossey-Alaoui, G. Su, E. Malaj, B.A. Roe and J.K. Cowell.
WAVE3, an actin-polymerization gene, is truncated and
inactivated as a result of a constitutional t(1;13)(q21;q12)
chromosome translocation in a patient with ganglioneuroblastoma.
Oncogene 21(38):5967-74 (2002)
E.S. Srivatsan, R. Chakrabarti, K. Zainabadi, S.D. Pack,
P. Benyamini, M.S. Mendonca, P.K. Yang, K. Kang, D. Motamedi,
M.P. Sawicki, Z. Zhuang, R.A. Jesudasan, U. Bengtsson,
C. Sun, B.A. Roe, E.J. Stanbridge, S.P. Wilczynski and
J.L. Redpath. Localization of deletion to a 300 Kb interval
of chromosome 11q13 in cervical cancer. Oncogene 21(36):5631-42
(2002)
K. Rithidech, J.J. Dunn, B.A. Roe, C.R. Gordon and E.P.
Cronkite. Evidence for two commonly deleted regions on
mouse chromosome 2 in gamma ray-induced acute myeloid
leukemic cells. Exp Hematol 30(6):564-70 (2002)
H. Wang, B. Ding, C.J. Liu, X.Y. Ma, S. Deschamps, B.A.
Roe and P. Lengyel. The Increase in Levels of Interferon-Inducible
Proteins p202a and p202b and RNA-Dependent Protein Kinase
(PKR) During Myoblast Differentiation Is Due to Transactivation
by MyoD: Their Tissue Distribution in Uninfected Mice
Does Not Depend on Interferons. J Interferon Cytokine
Res 22(6):729-37 (2002)
J. J. Iandolo, V. Worrell, K.H. Groicher, Y. Qian, R.
Y. Tian, S. Kenton, A. Dorman, H-G. Jia, S. Lin, P. Loh,
S. Qi, H. Zhu and B.A. Roe. Comparative analysis of the
genomes of the temperate bacteriophages phi 11, phi 12
and phi 13 of Staphylococcus aureus 8325. Gene 2002 May
1;289(1-2):109-18
Q. Zhang, W. Li, E.K. Novak, A. Karim, V.S. Mishra, S.F.
Kingsmore, B.A. Roe, T. Suzuki and R.T. Swank. The gene
for the muted (mu) mouse, a model for Hermansky-Pudlak
syndrome, defines a novel protein which regulates vesicle
trafficking. Hum Mol Genet 2002 Mar 15;11(6):697-706
G. Szalai, G. Duester, R. Friedman, H. Jia, S. Lin, B.A.
Roe and M.R. Felder. Organization of six functional mouse
alcohol dehydrogenase genes on two overlapping bacterial
artificial chromosomes. Eur J Biochem 2002 Jan;269(1):224-32
R.E. Broughton, J.E. Milam and B.A. Roe. Complete Nucleotide
Sequence of the Zebrafish (Danio rerio) Mitochondrial
Genome and Evolutionary Patterns in Vertyebrate Mitochondrial
DNA. Genome Research 11, 1958-1967 (2001).
T. Suzuki, W. Li, Q. Zhang, E.K. Novak, E.V. Sviderskaya,
A. Wilson, D. C. Bennett, B.A. Roe, R.T. Swank and R.A.
Spritz. The gene mutated in cocoa mice, carrying a defect
of organelle biogenesis, is a homologue of the human Hermansky-Pudlak
syndrome-3 gene. Genomics 78(1-2):30-7 (2001).
I. Tapia-Paez, M. Kost-Alimova, P. Hu, B.A. Roe, E. Blennow,
L. Fedorova, S. Imrek, and J.P. Dumanski. The position
of t(11;22)(q23;q11) constitional translocation breakpoint
is conserved among its carriers. Human Genetics. 109,
167-177 (2001).
O. B. Chernova, A. Hunyadi, E. Malaj, H. Pan, C. Crooks,
B. Roe and J. K. Cowell. A novel member of the WD-repeat
gene family, WDR11, maps to the 10q26 region and is disrupted
by a chromosome translocation in human glioblastoma cells.
Oncogene 20, 5378-5392 (2001).
T.K. Footz, P. Brinkman-Mills, G.S. Banting, S.A. Maier,
M. A. Riazi, L. Bridgland, S. Hu,, B. Birren, S. Minoshima,
N. Shimizu, H.Q., Pan, T. Nguyen, F. Fang, Y. Fu, L. Ray,
H. Wu, S. Shaull, S. Phan, Z. Yao, F. Chen, A. Hua, P.
Hu, Q. Wang, P. Loh, S. Qi, B.A. Roe and H.E. McDermid.
Analysis of the cat eye syndrome critical region in humans
and the region of conserved synteny in mice: A search
for candidate genes at or near the human chromosome 22
pericentromere. Genome Research 11, 1053-1070 (2001).
M. Levine, A. Progulske-Fox, N.D. Denslow, W.G. Farmerie,
D.M Smith, W.T. Swearingen, F.C. Miller, Z. Liang, B.A.
Roe and H-Q. Pan., Identification of Lysine decarboxylase
as a Mammalian Cell Growth Inhibitor in Eikenella corrodens:
Possible Role in Periodontal Disease. Microbial Pathogens
30, 179-192 (2001).
W. Ji, F. Chen, T. Do, A. Do, B. A. Roe and M. H. Meisler.
DQX1, an RNA dependent ATPase homolog with a novel DEAQ
box: expression pattern and genomic sequence comparison
of the human and mouse genes. Mammalian Genome 12, 456-461
(2001).
J.J. Ferretti, W.M. McShan, D. Ajdic, D. J. Savic, G.
Savic, K. Lyon, S. Sezate, A. N. Suvorov, C. Primeaux,
S. Kenton, H. Lai, S. Lin, Y., Qian, H. Jia, H. Zhu, Q.
Ren, F.Z, Najar, L. Song, J. White, X. Yuan, S. W. Clifton,
B. A. Roe, R. McLaughlin. Complete Genome Sequence of
an M1 Strain of Streptococcus pyogenes Proc. Natl. Acad.
Sci. USA. 98, 4658-4663 (2001).
H. Zhu, M. Nowrousian, D. Kupfer, H.V. Colot, G. Berrocal-Tito,
H. Lai, D. Bell-Pedersen, B.A. Roe, J.J. Loros, J.C. Dunlap.
Analysis of Expressed Sequence Tags From Two Starvation,
Time-of-Day-Specific Libraries of Neurospora crassa Reveals
Novel Clock-Controlled Genes. Genetics. 157, 1057-1065
(2001).
E.S. Lander, J. Rogers, R. H. Waterson, T. Hawkins, R.
Gibbs, Y. Sakaki, J. Weissenbach, D. R. Smith, A. Rosenthal,
H. Yang, L. Hood, R., W. Davis R. M. Myers, M. V. Olson,
N. Shimizu, G. A. Evans, B. A. Roe, J. Ramser, W. R. McCombie,
H. Blocker, R. Agarwala, F. Collins and other members
of the International Human Genome Sequencing Consortium.
Initial Sequencing and Analysis of the Human Genome. Nature
409, 860-921 (2001).
E. Dawson , Y. Chen, S. Hunt, L.J. Smink, A. Hunt, K.
Rice, S. Livingston, S. Bumpstead, R. Bruskiewich, P,
Sham, R. Ganske, M. Adams, K. Kawasaki, N. Shimizu, S.
Minoshima, B. Roe, D. Bentley, I. Dunham. A SNP Resource
For Human Chromosome 22: Extracting Dense Clusters of
SNPs from the Genomic Sequence. Genome Research, 11, 170-178
(2001).
E. Kitamura, G. Su, K. Sossey-Alaoui, E. Malaj, J. Lewis,
H. Pan, L. Hawthorn, B.A. Roe and J. K. Cowell A transcription
map of the minimally deleted region from 13q14 in B-cell
chronic lymphocytic leukemia as defined by large scale
sequencing of the 620 kb critical region. Oncogene, 19,
5772-5780 (2000).
P.L. Strissel, R. Strick, R.J. Tomek, B.A. Roe, J.D. Rowley
and N.J. Zeleznik-Le. DNA structural properties of AF9
are similar to MLL and could act as recombination hot
spots resulting in MLL/AF9 translocations and leukemogenesis.
Human Molecular Genetics, 9, 1671-1679 (2000).
M. Pletcher, B. A. Roe, F. Chen, T. Do, A. Do, E. Malaj
and R. Reeves. Chromosome evolution: The junction of mammalian
chromosomes in the formation of mouse chromosome 10. Genome
Research. 10, 1463-1467 (2000).
A. Raas-Rothschild, V. Cormier-Daire, M. Bao, E. Genin,
R. Salomon, K. Brewer, M. Zeigler, H. Mandel, S. Toth,
B. Roe, A. Munnich, and W.M. Canfield. Molecular basis
of variant pseudo-hurler polydystrophy. J. Clinical Investigation
105, 673-681 (2000).
M. Siniscalco, R. Robledo, S. Orru, L. Contu, P. Yadav,
Q. Ren, H. Lai, and B. Roe. A plea to search for deletion
polymorphism through genome scans in populations. Trends
in Genetics 16, 435-467 (2000).
I. Tapia-Paez, K.P. O'Brien, M. Kost-Alimova, S. Sahlen
S, D. Kedra, C.E. Bruder, B. Andersson, B.A. Roe, P. Hu,
S. Imreh, E. Blennow, and J.P. Dumanski. Fine mapping
of the constitutional translocation t(11;22). Hum. Genet.
106, 506-516 (2000).
C.J. Liu, H. Wang, Z. Zhao, S. Yu, Y. Lu, J. Meyer, G,
Chatterjee, S. Deschamps, B.A. Roe, and P. Lengyel. MyoD-Dependent
Induction during Myoblast Differentiation of p204, a Protein
Also Inducible by Interferon. Mol. Cell. Biol. 20, 7024-7036
(2000).
H. Kurahashi, T.H. Shaikh, P. Hu, B.A. Roe, B.S. Emanuel,
and M.L. Budarf. Regions of genomic instability on 22q11
and 11q23 as the etiology for the recurrent constitutional
t(11;22) Human Molecular Genetics 9, 1665-1670,(2000).
R.J. Moreland, M.E. Dresser, J.S. Rodgers, B.A. Roe, J.W.
Conaway, R.C. Conaway and J.S. Hanas. Identification of
a transcription factor IIIA-interacting protein. Nucleic
Acids Research 28, 1986-1993 (2000).
J. R. Korenberg, X-N. Chen, H. Hirota, Z. Lai, U. Bellugi,
D. Burian, B. Roe and R. Matsuoka. Genome Structure and
Cognitive Map of Williams Syndrome. J. Cognitive Neuroscience
12, 89-107, 2000. D. V. Santi, M. A. Siani, B. Julien,
D. Kupfer and B. Roe. An approach genes: a search for
the epothilone gene cluster. Gene 247, 97-102 (2000).
M.A. Riazi, P. Brinkman-Mills, T. Nguyen, H. Pan, S. Phan,
F. Ying, B. A. Roe, J. Tochigi, Y. Shimizu, S. Minoshima,
N. Shimizu, M. Buchwald, and H.E. McDermid. The human
homologue of insect-derived growth factor, CECR1, is a
candidate gene for features of cat eye syndrome. Genomics
64, 277-285 (2000).
M. Luijten, Y.P. Wang, B.T. Smith, A. Westerveld, L.J.
Smink, I, Dunham, B.A. Roe and T.J. Hulsebos. Mechanism
of spreading of the highly related neurofibromatosis type
1 (NF1) pseudogenes on chromosomes 2, 14 and 22. European
Journal of Human Genetics 8, 209-214 (2000).
K.L. Hester, J. Lehman, F. Najar, L. Song, B.A. Roe, C.H.
MacGregor, P.W. Hager, P.V. Phibbs and J.R. Sokatch. Crc
Is Involved in Catalobite Repression Control of the bkd
Operons of Pseudomonas putida and Pseudomonas aeruginosa.
J. Bacteriology 182, 1144-1149 (2000).
J. Lund, F. Chen. A. Hua, B. Roe, M. Budarf, B.S. Emanuel
and R.H. Reeves. Comparative Sequence Analysis of 634Kbp
of the Mouse Chromosome 16 Region of Conserved Synteny
with the Human Velocardiofacial Region of Chr 22q11.2.
Genomics 63. 374-383 (2000).
T.H. Shaikh, H. Kurahashi, S.C. Saitta, A. M. O'Hare,
P. Hu, B.A. Roe, D.A. Driscoll, D.M. McDonald-McGinn,
E.H. Zackai, M.L. Budarf and B.S. Emanuel. Chromosome
22-specific low copy repeats and the 22q11.2 deletion
syndrome: genomic organization and deletion endpoint analysis.
Human Molecular Genetics, 9(4), 489-501 (2000).
G. Glusman, A. Sosinsky, E, Ben-Asher, N. Avidan, D. Sonkin,
A. Bahar, A. Rosenthal, S. Clifton, B. Roe, C. Ferraz,
J. Demaille, and D. Lancet. Sequence, Structure, and Evolution
of a Complete Human Olfactory Receptor Gene Cluster. Genomics
63(2): 227-245 (2000).
J.Y. Zhou, B. Fogelgren, Z. Wang, B. A. Roe and J. A.
Biegel. Isolation of genes from the rhabdoid tumor deletion
region in chromosome band 2q11.2 Gene 241, 133-141 (2000).
I. Dunham, N. Shimizu, B.A. Roe, S. Chissoe, et. al. The
DNA Sequence of Human Chromosome 22. Nature 402, 489-495
(1999).
University of Oklahoma Department of Chemistry and Biochemistry 620 Parrington Oval, Rm 208 Norman, OK 73019-3051
|