Philip Leonard 'Len' Townes was born February 18, 1927 in Salem, Massachusetts to Saul and Lillian Townes. He graduated from Salem High School and attended Harvard University before enlisted in the United States Navy during World War II. After an honorable discharge at the end of the War, he completed his studies at Harvard, earning an AB in 1948. He went on to the University of Rochester, earning a PhD in 1952 under the mentorship of Johannes Holtfreter, and earning an MD in 1959. He completed his residency training in pediatrics at the University of Rochester in 1964 and served as Chief Resident in 1965.
Research
As a graduate student working in the laboratory of Johannes Holtfreter, Townes pioneered a technique for studying the kinetic and morphogenetic phenomena, subsequent to the combination of two or more well defined cell types, that revolutionized the understanding of morphogenesis, and serves as the basis for the differential adhesion hypothesis. With this technique, areas of embryonic tissue were teased from the embryos with glass needles. Once separated they could be recombined with one another. This demonstrated that in the process of sorting out, the different cell types exhibited a cell-specific tendency to arrange themselves in a definite tissue pattern that corresponded to that in normal development. The work was published as Townes' thesis in the classic paper in embryology and developmental biology, 'Directed movements and selective adhesion of embryonic amphibian cells' in 1955 in the J. Exp. Zool.128:53-120.
Medical career
Townes was a member of the faculty at the University of Rochester in the Departments of Anatomy and Pediatrics from 1952-1979. He was named Professor of Pediatrics in 1966 and served as the Chairman of the Division of Genetics and Director of the Genetic Clinic from 1966 to 1979. He served as an honorary research assistant at the University College, London, England between 1965 and 1966. In 1965, Townes described the first patient with isolated trypsinogen deficiency with secondary lack of activation of chymotrypsin and procarboxypeptidase. The 6-week old infant was unable to hydrolyze dietary protein due to a singular deficiency of pancreatic trypsinogen. This inborn error of metabolism, resulting in failure to thrive, became known as trypsinogen deficiency disease. In 1972, he identified a rare inherited syndrome in a father and four of his six children, characterized by the triad of imperforate anus, dysplastic ears, and thumb malformations, subsequently known as Townes-Brocks syndrome. Townes-Brocks syndrome was later found to be caused by a mutation in the DACT1 gene on chromosome 14q23. Townes was a member of the faculty and Professor of Pediatrics and Obstetrics and Gynecology at the University of Massachusetts Medical School from 1979-1995 where he directed the Genetic Clinic and the Cytogenetics Laboratory. In 1995 he retired to become an emeritus Professor of Pediatrics and Obstetrics and Gynecology.
