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Sargent, Tom

Formal Title:

Senior Investigator

Responsibilities:

Head of the Section on Vertebrate Development.

Phone:

301-496-0369

Email:

sargentt@mail.nih.gov

Address:

6 CENTER DR Room 4B412, MSC 2790
Bethesda Md 20892-2790
For FedEx use:
Bethesda Md 20892

Topics in my portfolio:

Biosketch:

Tom Sargent received his Bachelor of Arts degree in 1975 from Indiana University and his Ph.D. in Biochemistry from Caltech in 1981. He was a postdoc in Igor Dawid's lab at NIH, and has been a tenured scientist in the National Institute of Child Health and Human Development (NICHD) since 1989. Dr. Sargent's research interests have been in vertebrate developmental biology, and he has made many contributions, including production of one of the first mammalian genomic libraries (Sargent et al., 1979), and one of the first subtracted cDNA libraries (Sargent and Dawid, 1983). Dr. Sargent and colleagues were the first to demonstrate the requirement for cell-cell communication in mesoderm formation in the frog embryo (Sargent et al., 1986), and that dissociation of frog embryonic cells could trigger neural development (Sato and Sargent, 1989). The Sargent lab discovered the role of the transcription factor AP-2 in regulating epidermal gene expression (Snape et al., 1991), the function of Eph class receptors in regulating cell adhesion (Winning et al., 1996), and the roles of the Dlx3 gene in epidermal (Morasso et al., 1996) and placental (Morasso et al., 1999) development in the mouse. His lab also showed that TFAP2 is required for induction of neural crest in Xenopus, and used this to identify downstream target genes that are important in neural crest development.  In addition to his work at NIH, Dr. Sargent has been an Associate Clinical Professor in the Institute for Biomedical Sciences at The George Washington University, in Washington, D.C. where he has taught courses in molecular biology and medical genetics.

Publications (PubMed):

Maternal pak4 expression is required for primitive myelopoiesis in zebrafish.
Generation and characterization of a novel neural crest marker allele, Inka1-LacZ, reveals a role for Inka1 in mouse neural tube closure.
Inca: a novel p21-activated kinase-associated protein required for cranial neural crest development.
Myosin-X is required for cranial neural crest cell migration in Xenopus laevis.
Transcriptional regulation at the neural plate border.
PCNS: a novel protocadherin required for cranial neural crest migration and somite morphogenesis in Xenopus.
Msx1 and Msx2 have shared essential functions in neural crest but may be dispensable in epidermis and axis formation in Xenopus.
Expression of TFAP2beta and TFAP2gamma genes in Xenopus laevis.
Developmental expression of Xenopus fragile X mental retardation-1 gene.
Regulatory targets for transcription factor AP2 in Xenopus embryos.
AP-2alpha selectively regulates fragile X mental retardation-1 gene transcription during embryonic development.
Induction of neural crest in Xenopus by transcription factor AP2alpha.
Transcription factor AP-2 is an essential and direct regulator of epidermal development in Xenopus.
Vision National Institutes of Health Home BOND National Institues of Health Home Home Storz Lab: Section on Environmental Gene Regulation Home Machner Lab: Unit on Microbial Pathogenesis Home Division of Intramural Population Health Research Home Bonifacino Lab: Section on Intracellular Protein Trafficking Home Lilly Lab: Section on Gamete Development Home Lippincott-Schwartz Lab: Section on Organelle Biology