The Wayne State University Board of Governors approved the university-wide Center for Molecular Medicine and Genetics (CMMG) effective Oct. 1, 1994. Its mission is to enhance research strength in molecular medicine and genetics at WSU and to develop interdisciplinary research and training programs in targeted human health areas that bridge basic and clinical science. By promoting interactions and collaborations throughout the university and its affiliated hospitals, CMMG programs should provide new opportunities for external funding and foster translational research and technology transfer.
The CMMG currently has 19 primary, 9 joint, and 6 associate/adjunct faculty members. The majority of the CMMG faculty also have appointments and close associations with clinical departments. In addition to their individual research programs, the CMMG faculty are developing interdisciplinary programs with clinical scientists in areas such as human genetics and gene therapy, cancer, AIDS, neurological diseases and human reproductive biology. These interactions and collaborations include faculty in the WSU departments of Internal Medicine, Neurology, Pathology, Obstetrics and Gynecology, Surgery, Pediatrics, Emergency Medicine, Urology, and Psychiatry and Behavioral Neurosciences. Joint publications and research grant applications have resulted from some of these collaborative efforts.
The CMMG is broadening its academic programs to make them more interdisciplinary and to provide new opportunities for medical, graduate and postdoctoral student research in more clinically oriented areas. The number of faculty participating in the existing molecular biology and genetics graduate program has more than doubled in the last two years. More graduate students are carrying out their doctoral research in clinical departments. A proposal for a new M.S. degree program in genetic counseling has been submitted for approval and a program director has been hired. Other new graduate programs are being developed. Focused training programs and research opportunities for medical students, residents, fellows and clinical faculty will be offered, including courses and workshops on techniques, methodologies and research approaches in molecular medicine and genetics.
An important CMMG goal is to promote communication and interaction with medical biotechnology companies to facilitate the application of discovery research to the prevention, diagnosis and treatment of diseases, and to promote economic development in the state of Michigan.
The CMMG is providing research training opportunities for residents, fellows and faculty from several clinical departments and intends to expand these opportunities as the center continues to grow and develop. It has a Macromolecular Core Facility for nucleic acid synthesis and sequencing, and a shared Biocomputing Facility that have been used extensively by faculty and students in more than a dozen departments, centers, and institutes. CMMG faculty and staff are also available for advice and strategy in the design and interpretation of experiments involving molecular and cellular approaches.
"Faculty interested in a CMMG appointment should send an application letter and curriculum vitae to the director at 3216 Scott Hall ..."
Many of the CMMG goals and programs are prospective in nature since the center is in the early stages of its development. The implementation and achievement of these future objectives will be greatly facilitated by the involvement and participation of faculty and students throughout the university and its affiliated hospitals, who are strongly encouraged to become involved with center programs and activities. Faculty interested in a CMMG appointment should send an application letter and curriculum vitae to the director at 3216 Scott Hall (telephone 313-577-5323).
John Tomkiel, Ph.D., joined the CMMG in November of 1994 as an assistant
professor from the Johns Hopkins University School of Medicine where he
completed a postdoctoral fellowship. His tenure-retreat department is
biological sciences. He received his Ph.D. in genetics in 1990 from the
University of Washington. Dr. Tomkiel's research focus is the function of
the centromere in cell division and its aberration in cancer and birth
defects.
Anne Greb, M.S., became an assistant professor in the CMMG in January of
1995 on the clinical-educator track. She is the director of the Genetic
Counseling Graduate Program that is currently being reviewed for approval
as a new master's program. Professor Greb trained at the University of
Wisconsin, Madison, and has been a staff genetic counselor since 1986,
with six of those years at Hutzel Hospital, where she participated in the
medical teaching program of the Reproductive Genetics Unit.
Robert A. Thomas, Ph.D., was promoted in May 1995 to assistant professor
(research) after completing a postdoctoral fellowship in the CMMG. He
received his Ph.D. from the department of biological sciences at WSU in
1992. Dr. Thomas's research using HIV-1 to study the infection and
transcriptional activation of retroviruses in human fetal development in
collaboration with Drs. A. Scott Goustin (CMMG), Theodore Jones
(Obstetrics-Gynecology) and James Jarvis (Pediatrics) will be extended to
include HIV-2.
S. Helena Kuivaniemi, M.D./Ph.D., joined the CMMG in September of 1995 as
a tenure-track associate professor with tenure-retreat in the department
of surgery. She came from Jefferson Medical College at Thomas Jefferson
University in Philadelphia where she worked on the molecular basis of a
number of connective tissue disorders and, more recently, of aortic
aneurysms. Her studies in that area focused on the candidate gene
approach and led to the identification of mutations in the gene for type
III procollagen that were associated with aortic aneurysms in some
families. At WSU, Dr. Kuivaniemi, in collaboration with Professor Anne
Greb, and Drs. Ramon Berguer, Andris Kazmers and Ronald Kline (surgery),
will continue to collect familial cases of abdominal aortic aneurysms in
order to use DNA linkage analysis to identify the gene(s) involved in the
development of aneurysms. Her work will also include differential display
PCR to identify unique genes expressed in the aorta.
Gerardus Tromp, Ph.D., joined the CMMG as an assistant professor
(research) in September, 1995. He came from Thomas Jefferson University
in Philadelphia, where he was a research assistant professor. Dr. Tromp
received his Ph.D. in 1989 from Rutgers University and completed his
postdoctoral training at Jefferson Medical College. His research involved
defining the molecular basis of several connective tissue disorders such
as osteogenesis imperfecta and variants of the Ehlers Danlos syndrome.
Recently, he has worked on intracranial aneurysms, attempting to define
the gene(s) predisposing individuals to the disease, initially by using
the candidate gene approach and subsequently by genetic epidemiology and
linkage. At WSU, in collaboration with Dr. Antti Ronkainen (currently at
WSU), members of the neurosurgery department, and the University of
Kuopio, Finland, he will continue to collect information on families with
intracranial aneurysms to define the gene or genes that predispose the
disease by using linkage analyses. Furthermore, he hopes to establish
other collaborative projects with WSU faculty involving genetic
epidemiology and linkage.
Russell L. Finley, Jr., Ph.D., came from the Harvard Medical School
Department of Genetics in September 1995 as an assistant professor in the
CMMG with tenure-retreat in the department of internal medicine,
hematology/oncology division. He had trained at the Massachusetts General
Hospital following his Ph.D. training (1990) at State University of New
York, Syracuse. Dr. Finley will continue his research on understanding
the regulatory networks that control cell proliferation during
development, employing a powerful genetic interaction trap methodology
that he helped develop, along with conventional molecular and genetic
techniques.
James Garbern, M.D./Ph.D., became a joint assistant professor in the CMMG
and neurology department in September 1995. He came from the University
of Pennsylvania School of Medicine where he had been an assistant
professor studying the molecular genetics of neurological disease. Dr.
Garbern carried out his medical, doctoral and postdoctoral training at
Baylor College of Medicine and the National Institutes of Health. At WSU,
his research focus is the cloning and analysis of human genes involved in
the regulation of myelination. Dr. Garbern is currently organizing a
Neurogenetics Center at WSU with Professor Greb and Dr. Kamholz.
In addition to the new primary faculty, we welcome the following new
associate faculty members: James Jarvis, M.D. (pediatrics), Donald Kuhn,
Ph.D. (psychiatry and behavioral neurosciences), Kenneth Maiese, M.D.
(neurology), Adnan Munkarah, M.D. (obstetrics and gynecology), and
Michael Shy, M.D. (neurology).
We offer further congratulations for recent MBG Ph.D. recipient Chris
Krebs, who won the Duncan McCarthy Award for the best comprehensive
abstract submitted by a student or postdoc to the annual (1995) meeting of
the Michigan Chapter of Neurosciences.
"The CMMG is broadening its academic programs to make them more
interdisciplinary and to provide new opportunities ..."
The CMMG has also formulated a Genetic Counseling Graduate Program (with
Prof. Anne Greb as director) that is currently under review by the
Graduate School. The objective of the program is to provide students with
the skills to function as productive and responsible genetic counselors in
a variety of work settings. Students will have the opportunity to
interact with numerous clinical genetic professionals including genetic
counselors, pediatric and obstetrical medical geneticists,
cytogeneticists, and biochemical and molecular geneticists. The program
is designed to meet the criteria for accreditation by the American Board
of Genetic Counseling, and will therefore integrate scientific knowledge
and counseling skills with different clinical experiences. The course
work consists of: principles of human and medical genetics, molecular
biology, and counseling and interviewing skills. Students will obtain
supervised clinical experience in a variety of genetics and subspecialty
clinics, as well as in genetic service laboratories throughout The Detroit
Medical Center and surrounding hospitals. Pending its approval as a new
graduate program, it will admit the first class of four students for the
fall of 1996.
1. Availability of genetic testing for specific diseases;
The CMMG is also committed to continuing education for health care
providers and those in training regarding the implications of genetic
testing, and is available for inservices and other educational programs.
For more information please contact Professor Anne Greb at 313-577-6298 or
agreb@cmb.biosci.wayne.edu
Leon Carlock, associate professor (also with anatomy and cell biology);
Ph.D., Purdue, 1981. Molecular neurobiology; Huntington's disease;
neuron-specific gene expression in the caudate nucleus.
Mark I. Evans, Professor (also with Obstetrics and Gynecology); M.D., SUNY
Downstate Medical Center, 1978. Prenatal diagnosis and fetal therapy.
Craig N. Giroux, assistant professor (also with obstetrics and
gynecology); Ph.D., MIT, 1979. Cell and molecular biology of meiotic
differentiation; DNA and chromosome transactions in the germ line; genetic
stability and carcinogenesis; yeast biotechnology.
Morris Goodman, professor (also with anatomy and cell biology); Ph.D.,
Wisconsin, 1951. Molecular evolution, with emphasis on globin genes and
the X-linked HPRT gene.
Anton Scott Goustin, assistant professor (research); Ph.D., California
(Berkeley), 1979. Gene therapy; retroviral control of transcription;
natural inhibitors of tyrosine kinases; peptide growth factor receptors in
embryonic development.
Lawrence I. Grossman, associate director and professor (also with internal
medicine); Ph.D., Yeshiva (Einstein), 1971. Molecular biology of
mitochondria; cytochrome c oxidase genes; mitochondrial DNA.
George Grunberger, professor (also with internal medicine and director,
Diabetes Program); M.D., NYU, 1977. Molecular biology of insulin action;
insulin receptors; receptor gene expression in insulin resistance.
Mark Paul Johnson, associate professor (also with obstetrics and
gynecology); M.D., Minnesota, 1984. Prenatal diagnosis and fetal therapy.
Minoru S. H. Ko, assistant professor (research); M.D., 1986, Ph.D., 1991,
Keio (Japan). Mouse cDNA sequencing and mapping; human genome project;
molecular biology of implantation; genomic imprinting.
Stephen A. Krawetz, associate professor (also with obstetrics and
gynecology); Ph.D., Toronto, 1983. Gene therapy; control of development
and differentiation; expression of genes controlling spermatogenesis;
expression of connective tissue matrix genes in normal and pathological
development; computer-assisted sequence analysis.
Gyanendra Kumar, associate professor (also with neurology); Ph.D., Lucknow
(India), 1976. Molecular biology of human papovavirus JC; regulation of
eukaryotic gene expression.
Markku Kurkinen, professor (also with pathology); Ph.D., Helsinki, 1979.
Extracellular matrix; metalloproteinases; gene regulation; development.
Wayne Lancaster, professor (also with obstetrics and gynecology); Ph.D.,
Wayne State, 1973. Papillomaviruses: molecular biology, evolution, and
role in human carcinogenesis.
Leonard C. Lutter, adjunct associate professor (also with Henry Ford
Hospital); Ph.D., Wisconsin, 1973. Characterization of cellular and viral
transcription complexes.
Dorothy A. Miller, professor (also with pathology); Ph.D., Yale, 1957.
Molecular cytogenetics; mammalian centromeres; in situ hybridization; gene
mapping.
Orlando J. Miller, professor (also with obstetrics and gynecology); M.D.,
Yale, 1950. Molecular cytogenetics; role of CpG-rich islands and DNA
methylation in gene regulation; chromosome structure, genome organization,
and gene amplification.
Richard E. Miller, professor (also with internal medicine and associate
chief of staff for research and development, Veterans Administration
Medical Center); M.D., Michigan, 1966. Study of gene expression during
differentiation; transcription of insulin gene.
Jeffrey Moshier, assistant professor (also with internal medicine); Ph.D.,
Johns Hopkins, 1984. Molecular oncology; gene expression; role of
polyamines and ornithine decarboxylase in tumorigenesis.
Mary T. Murray, assistant professor (research); Ph.D., MIT, 1987.
Translational regulation of gene expression; germ line differentiation and
early embryogenesis; RNA-protein interactions.
Robert H. Rownd, director and professor (also with internal medicine);
Ph.D., Harvard, 1964. Gene therapy; retroviral vectors; structure,
function, and replication of the genetic elements; cellular regulatory
mechanisms; gene amplification.
J. Christopher States, assistant professor (research); Ph.D., Albany
Medical College, Union University, 1980. Genetics of human DNA repair;
bioactivation of carcinogens; gene therapy.
Anton Scott Goustin, "HIV infection of developing placenta," Theodore B.
Jones, M.D., obstetrics and gynocology, Fayth Yoshimura, Ph.D., and Steven
R. King, Ph.D., immunology; "Natural insulin receptor tyrosine kinase
inhibitor," Myron A. Leon, Ph.D., immunology, George Grunberger, M.D., and
Pothur R. Srinivas, M.D., internal medicine; "Gene therapy to expand
hematopoietic stem cells," Alan W. Flake, M.D., surgery, Fayth Yoshimura,
Ph.D., and Steven C. Lerman, Ph.D., immunology.
Lawrence I. Grossman, "Molecular events in neuronal ischemic-reperfusion
injury," Blaine C. White, M.D., and Gary Krause, M.D., emergency medicine.
George Grunberger, "Structure-function relationships of a human insulin
receptor tyrosine kinase inhibitor," Myron Leon, Ph.D., immunology; "The
use of insulin harmonic waveform analysis in the evaluation of pulsatile
insulin secretion in patients with Type II diabetes mellitus," Michael
Diamond, M.D., and Ralph Kramer, M.D., obstetrics and gynecology.
Minoru S. H. Ko, "Genetics of skin diseases," Ken Hashimoto, M.D.,
dermatology.
"CMMG faculty are developing interdisciplinary programs with clinical
scientists in areas such as human genetics and gene therapy ..."
S. Helena Kuivaniemi, "Familial abdominal aneurysms," Ramon Berguer, M.D.,
Andris Kazmers, M.D., and Ronald A. Kline, M.D., surgery.
Markku Kurkinen, "Role of proteases in breast cancer progression," Rafael
Fridman Ph.D., pathology; "Matrix metalloproteinases in arthritis and
other degenerative diseases," Felix Fernandez-Madrid, M.D./Ph.D.,
rheumatology.
Wayne Lancaster, "Human papillomavirus in head and neck cancers," John
Ensley, M.D., internal medicine, hematology-oncology; "Identification of
tumor suppressor genes in ovarian cancer; expression of T-Cell receptor
usage in cervical cancer; Role of virus in ovarian cancer," Adnan
Munkarah, M.D., obstetrics-gynecology; "Association between clinical
course of aids and Class II HLA," Jack Sobel, M.D. and Paula Shuman, M.D.,
internal medicine, infectious diseases.
Jeffrey Moshier, "Gastric mucosal injury and aging; Aging and induction of
colorectal neoplasia," Adhip Majumdar, Ph.D./D.Sc., internal medicine and
biochemistry; "Early weaning and gut development - Role of ornithine
decarboxylase and tyrosine kinases," Chuan- Hao Lin,, M.D., pediatric
gastroenterology; "The efficacy of thymosin Alpha-1 in the treatment of
chronic Hepatitis B disease, Thymosin Alpha-1 bioassays utilizing
Hepatitis B transfected hepatoma cells," Milton Mutchnick, M.D. and Paul
Naylor, Ph.D., internal medicine.
Mary T. Murray, "Apoptosis during kidney reperfusion injury," Scott
Dulchavsky, M.D., surgery, and Ken Palmer, Ph.D., pathology.
Robert H. Rownd, "Gene therapy," Lawrence Lum, M.D., formerly of internal
medicine, hematology-oncology, and currently scientific director of The
Adoptive Immunotherapy/Gene Therapy Program at St. Luke's Medical Center
in Milwaukee, Wis.
J. Christopher States, "Cellular and molecular toxicity of lead," Joel G.
Pounds, Ph.D., institute of chemical toxicology; "Gene therapy approaches
for Parkinson's disease," Donald M. Kuhn, Ph.D., psychiatry.
Robert A. Thomas, "HIV transcriptional activation," Theodore Jones, M.D.,
obstetrics and gynecology; "Involvement of HIV immune complexes in
vertical transmission," James Jarvis, M.D., pediatrics.
"The CMMG has a Macromolecular Core Facility and a shared Biocomputing
Facility that have been used by faculty and students in more than a dozen
departments, centers, and institutes..."
Carlock, L., Walker, P.D., Shan, Y., and Gutridge, K. 1995. Transcription
of the Huntington disease gene during the quinolinic acid excitotoxic
cascade. NeuroReport 6:1121-1124.
Evans, M.I., Chik, L., O'Brien, J.E., Chen, B., Dvorin, E., Ayoub, M.,
Krivchenia, E.L., Ager, J.W., Johnson, M.P., and Sokol, R.J. 1995. MOMs
and DADs: improved specificity and cost effectiveness of biochemical
screening for aneuploidy with DADs. Am. J. Obstet. Gyn. 172:1138-1147.
Evans, M.I., Littman, L., St. Louis, L., LeBlanc, L., Adis, J., Johnson,
M.P., and Moghissi, K.S. 1995. Evolving patterns of iatrogenic multifetal
pregnancy generation: implications for aggressiveness of infertility
treatments. Am. J. Obstet. Gyn. 172:1750-1753.
Greb, A.E., Sepulveda, W., Romero. R., Treadwell, M.C., Johnson, M.P., and
Evans, M.I. 1995. Isolated fetal choroid plexus cyst: karyotyping is
indicated. (submitted).
Gregoire L., Cubilla, A.L., Reuter, V.E., Haas, G.P., and Lancaster, W.D.
1995. Penile invasive squamous cell carcinoma: human papillomavirus
preferentially associated with high grade variants. J. Nat'l. Cancer
Inst. In press.
Grossman, L.I., Rosenthal, N., Akamatsu, M., and Erickson, R.P. 1995.
Developmental regulation of cytochrome c oxidase isoform expression in
mouse embryos. Biochem Biophys. Acta 1260:361-364.
Grossman, L.I. 1995. Mitochondrial mutations and human disease. Environ.
Mol. Mutagen 25:30-37.
Jaber, L.A., Slaughter, R.L., and Grunberger, G. 1995. Diabetes and
related metabolic risk factors among Arab Americans. Ann. Pharmaco. Ther.
29:573-576.
Ko, M.S.H. 1995. Equalized cDNA libraries. In Reverse Transcriptase PCR
(Larrick, J.W., and Siebert, P.D., Eds.) Simon and Schuster.
Kramer, J.A., and Krawetz, S.A. 1995 Matrix associated regions in haploid
expressed domains. Mamm. Genome 6:677-679.
Krebs, C.J., McAvoy, M., and Kumar, G. 1995. JC virus minimal core
promotion is glial specific in vivo. J. Virol. 69:2434-2442.
Kuivaniemi, H., Tromp, G., Bergfeld, W.F., Kay, M., and Helm, T.N. 1995.
Ehlers-Danlos syndrome type IV: A single base substitution of the last
nucleotide of exon 34 in COL3A1 leads to exon skipping. J. Invest.
Dermat. 105:352-356.
Kuivaniemi, H., Tromp, G., and Prockop, D.J. 1996. Genetic causes of
aortic aneurysms. In: Molecular Genetics and Gene Therapy of
Cardiovascular Diseases. (Mockrin, S.C., ed.) Marcel Dekker, Inc., New
York, pp.209-218.
Levy, J., Vandenberg, M., and Grunberger, G. 1995. Insulin versus
glipizide treatment in patients with non-insulin-dependent diabetes
mellitus. Effects on blood pressure and glucose tolerance. Am. J.
Hypertens. 8:445-453.
Miller, O.J. 1995. The fifties and the renaissance in human and
mammalian cytogenetics. Genetics 139:489-494.
Moshier, J.A., Malecka-Panas, E., Geng, H., Dosescu, J., Tureaud, J.,
Skunca, M., and Majumdar, A.P.N. 1995. Ornithine decarboxylase
transformation of NIH/3T3 cells is mediated by altered epidermal growth
factor receptor activity. Cancer Res. 55:5358-5365.
Nikolajczyk, B.S., Murray, M.T., and Hecht, N.B. 1995. A mouse homologue
of the Xenopus germ cell-specific ribonucleic acid/deoxyribonucleic
acid-binding proteins p54/p56 interacts with the protamine 2 promoter.
Biol. Repr. 52:524-530.
Porter, C. A., Sampaio, I., Schneider, H., Czelusniak, J., and Goodman, M.
1995. Evidence on primate phylogeny from epsilon globin gene sequences
and flanking regions. J. Mol. Evol. 40:30-55.
Quan, T.H., Reiners, J.J., Culp, S.J., Richter, P., and States, J.C.
1995. Differential mutagenicity and cytotoxicity of
(+/-)-benzo(a)pyrene-trans-7,8- dihydrodiol and
(+/-)-anti-benzo(a)pyrene-trans-7,8-dihydrodiol-9,10-epoxide in
genetically engineered human fibroblasts. Mol. Carcinogenesis 12:91- 102.
Ronkainen, A., Hernesniemi, J., and Tromp, G. 1995. Special features of
familial intracranial aneurysms: Report of 215 familial aneurysms.
Neurosurgery 37:43-47.
Seelan, R.S., Gopalakrishnan, L., Scarpulla, R.C., and Grossman, L.I.
1996. Cytochrome c oxidase subunit VIIa liver isoform: Characterization
and identification of promoter elements in the bovine gene. J. Biol.
Chem. 271:2112-2120.
Singh, G.B., and Krawetz, S.A. 1995. CLONEPLACER: A software tool for
simulating contig formation for OSS Ordered Shotgun Sequencing. Genomics
25:555-558.
Srinivas, P.R., Goustin, A.S., and Grunberger, G. 1995. Baculoviral
expression of a natural inhibitor of the human insulin receptor tyrosine
kinase. Biochim. Biophys. Res. Commun. 208:879-885.
Tomkiel, J., Fanti, L., Berloco, M., Spinelli, L., Tamkun, J.W., Wakimoto,
B.T., and Pimpinelli, S. 1995. Developmental genetical analysis and
molecular cloning of the abnormal oocyte gene of Drosophila melanogaster.
Genetics 140:615-627.
Topping, R.S., Myrand, S.P., Williams, B.L., Albert, J.C., and States,
J.C. 1995. Characterization of the human XPA promoter. Gene
166:341-342.
Tromp, G., De Paepe, A., Nuytinck, L., Madhatheri, S., and Kuivaniemi, H.
1995. Substitution of valine for glycine 793 in the triple-helical domain
of type III procollagen in a mother and a child with the Ehlers-Danlos
syndrome type IV. Hum. Mutat. 5:179-181.
Tugendreich, S., Tomkiel, J., Earnshaw, W.C., and Hieter, P. 1995. The
CDC27Hs protein co-localizes with the CDC16Hs protein to the centrosome
and mitotic spindle and is essential for the metaphase to anaphase
transition. Cell 81:261-268.
Wykes, S.M., Nelson, J.E., Visscher, D.W., Djakiew, D., and Krawetz, S.A.
1995 Coordinate expression of the PRM1, PRM2 and TNP2 multigene locus in
human testis. DNA Cell Biol. 14:155-161.
Zachar, V. , Goustin, A.S., Zacharova, V., Hager, H., Koppelhus, U.,
Womble, D.D., Liu, X., Bambra, C.S., Nyongo, A., and Ebbesen, P. 1996.
Genetic polymorphism of envelope V3 region of HIV type 1 subtypes A, C,
and D from Nairobi, Kenya. AIDS Res. Hum. Retroviruses 12:75-78.
CMMG Welcomes 13 New Faculty Members
John Kamholz, M.D./Ph.D., joined the CMMG as a joint associate professor
with tenure in the WSU Department of Neurology in the summer of 1994. Dr.
Kamholz had been an Assistant Professor at the University of Pennsylvania
School of Medicine, where he initiated studies on human myelin basic
protein gene regulation. Dr. Kamholz's recruitment provided a bridge
between the department of neurology and the CMMG that has been
strengthened with the recent recruitment of Dr. James Garbern.CMMG Graduate Training Programs
CMMG currently offers a graduate program in molecular biology and genetics
(MBG) with Ph.D. and master's degrees. Currently 25 students are enrolled
in the Ph.D. program, two of whom are M.D.-Ph.D. candidates, and two
master's candidates. In the past year CMMG has awarded 7 Ph.D. degrees
and two master's degrees. Our congratulations go to Drs. Scott Smith,
VijayaLaksmi Shridhar, Kristin Gutridge, Shiping Tang, William Paradee,
Timothy Drumheller, and Chris Krebs, who have gone on to promising
postdoctoral positions. We wish them all the best in their careers.
CMMG Activities
CMMG is a Clinical Genetics Resource
The Center for Molecular Medicine and Genetics is available to assist
health care providers in gathering the following information:
2. Disease-specific patient support groups;
3. Statewide clinical genetic services and specialty clinics.CMMG Faculty and Their Research
(For new faculty, see the article on page 2.)CMMG Research Collaborations
James Garbern, "Myelin gene expression as molecular markers for cerebral
tumors," Lucia Zamorano, M.D., neurosurgery, John Kamholz, M.D./Ph.D., and
Lisa Rogers, M.D., neurology. CMMG Co-Sponsors AIDS Symposium
The CMMG co-sponsored the Second Conference on AIDS Research at WSU with
the AIDS Research Advisory Committee, the dean of medicine, Harper
Hospital, and the University of Detroit Mercy School of Dentistry. More
than 100 participants attended the conference, which was held on Oct. 27,
1995 at Scott Hall. Seven WSU faculty and a faculty member from the
University of Detroit Mercy School of Dentistry made oral presentations on
current AIDS research. Twelve research groups presented posters on
clinical and basic AIDS research. CMMG Macromolecular Core Facility
The CMMG Macromolecular Core Facility, located in room 5177 of the
Biological Sciences Building, offers two services to researchers at Wayne
State University: DNA sequencing and DNA synthesis. The DNA sequencing is
accomplished using an Applied Biosystems DNA Sequencer. This instrument
uses four different fluorescent dyes (one for each base) to automate the
base calling of the sequencing gel. Two types of fluorescence labeling
are available: dye-labeled primers or dye-labeled terminators. Primers
available from the facility are M13 forward and reverse, SP6, T7 and T3.
Researchers provide the facility with their own primer for the second
methodology. Samples can be either plasmid (single or double stranded) or
PCR products. A normal gel run will produce about 400 base pairs per
sample. Data files of the results suitable for analysis by computer can
be provided. Each sequencing sample carries a $30 fee. The facility also
has an Applied Biosystems DNA Synthesizer for synthesizing oligonucleotide
primers and probes. However, this instrument has only modest production
capabilities. The Center is in the process of purchasing a Beckman
instrument with a significantly higher output capacity. For information
about this facility, please contact Mike Hagen, Ph.D., at 313-577-1178 or
mhagen@cmb.biosci.wayne.edu . CMMG Shared Biocomputing Facility
The CMMG maintains a shared Biocomputing Facility for the analysis of
molecular biological data. The facility runs on a Sun SPARCStation 20
that is connected to the WSU network and the Internet. The GCG Sequence
Package for analysis of peptide and nucleic acid sequence data and the
GenBank and EMBL databases are maintained locally. Several other tools
for data analysis are also available, as is direct connectivity to the
NCBI databases at NIH. The facility also provides Internet E-mail service
to all faculty, students and staff in the CMMG as well as to many members
of other departments in the WSU community. As part of its mission in
technology transfer, the CMMG also provides Internet access and E-mail
service to members of the Michigan Biotechnology Association. Currently,
no charges are associated with use of the CMMG shared Biocomputing
Facility. For more information, please contact David Womble, Ph.D., at
313-577-2374 or
dwomble@cmb.biosci.wayne.eduRepresentative Publications from CMMG Faculty
Bingham, P., Scott, M., Wang, S., McPhaul, M., Wilson, E., Garbern, J.,
Merry, D., and Fishbeck, K. 1995. Stability of an expanded trinucleotide
repeat in the androgen receptor gene in transgenic mice. Nature Genetics
9:191-196.
The CMMG News is edited by Mary T. Murray, Ph.D. (313-577-4346,
mmurray@cmb.biosci.wayne.edu), and David D. Womble, Ph.D. (313-577-2374,
dwomble@cmb.biosci.wayne.edu).
Center for Molecular Medicine and Genetics
Wayne State University School of Medicine
3216 Scott Hall
540 East Canfield
Detroit, MI 48201
313-577-5323
cmmg@cmb.biosci.wayne.edu