The MIT Center for Environmental Health Sciences is a multidisciplinary research organization which has taken as its primary mission the discovery of the relationship between human exposure to environmental chemicals, mutation, and genetic diseases such as cancer and birth defects. The Center faculty are integrated in six multidisciplinary research programs which address the sources, environmental movement and genetic effects of chemicals borne to humans by food, air and water. One of these, the Superfund Basic Research Program, involves study of chemical exposure and genetic change in the population of the nearby Aberjona River Basin. This major effort began with four years of public outreach activities and which continue in a public education program to explain the basis, potential value and limitations of our studies in this community in which many of our faculty and staff reside. The MIT academic departments represented by Center faculty include Toxicology (7), Civil Engineering (7), Chemical Engineering (5), Mechanical Engineering (7), Chemistry (2), Biology (2) and Earth and Planetary Sciences (1). Joining these several disciplines together are the shared Core Laboratories in Analytical Chemistry and Toxicology which permit analysis, testing and identification of the most important human mutagens in complex environmental mixtures. Key technologies developed at the Center include means to measure and identify chemicals in human tissue proteins and measurement of mutations and mutational spectra in human cells or tissues. These technologies now drive a transmutation of present core facilities and faculty research toward direct measurement of chemicals and patterns of genetic changes in human cells and tissues. Through these studies we hope to fulfill our primary mission and make a contribution to public health that will justify public support of work.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
5P30ES002109-23
Application #
6382062
Study Section
Environmental Health Sciences Review Committee (EHS)
Program Officer
Collman, Gwen W
Project Start
1978-07-01
Project End
2004-03-31
Budget Start
2001-04-01
Budget End
2002-03-31
Support Year
23
Fiscal Year
2001
Total Cost
$1,084,962
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Internal Medicine/Medicine
Type
Schools of Arts and Sciences
DUNS #
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Viswanathan, Srinivas R; Nogueira, Marina F; Buss, Colin G et al. (2018) Genome-scale analysis identifies paralog lethality as a vulnerability of chromosome 1p loss in cancer. Nat Genet 50:937-943
Winn, Caroline Bodi; Artim, Stephen C; Jamiel, Morgan S et al. (2018) Lung Lobe Torsion in an Adult Male Common Marmoset (Callithrix jacchus). Comp Med 68:314-318
Co, Julia Y; Cárcamo-Oyarce, Gerardo; Billings, Nicole et al. (2018) Mucins trigger dispersal of Pseudomonas aeruginosa biofilms. NPJ Biofilms Microbiomes 4:23
Keegan, Caroline; Krutzik, Stephan; Schenk, Mirjam et al. (2018) Mycobacterium tuberculosis Transfer RNA Induces IL-12p70 via Synergistic Activation of Pattern Recognition Receptors within a Cell Network. J Immunol 200:3244-3258
DiChiara, Andrew S; Li, Rasia C; Suen, Patreece H et al. (2018) A cysteine-based molecular code informs collagen C-propeptide assembly. Nat Commun 9:4206
Caron, Tyler J; Artim, Stephen C; Israelsen, William J et al. (2018) Cutaneous Dermatophilosis in a Meadow Jumping Mouse (Zapus hudsonius). Comp Med 68:25-30
Phillips, Angela M; Doud, Michael B; Gonzalez, Luna O et al. (2018) Enhanced ER proteostasis and temperature differentially impact the mutational tolerance of influenza hemagglutinin. Elife 7:
Wang, Xin; Garcia, Carlos T; Gong, Guanyu et al. (2018) Automated Online Solid-Phase Derivatization for Sensitive Quantification of Endogenous S-Nitrosoglutathione and Rapid Capture of Other Low-Molecular-Mass S-Nitrosothiols. Anal Chem 90:1967-1975
Moore, Christopher L; Papa 3rd, Louis J; Shoulders, Matthew D (2018) A Processive Protein Chimera Introduces Mutations across Defined DNA Regions In Vivo. J Am Chem Soc 140:11560-11564
Chan, Cheryl; Pham, Phuong; Dedon, Peter C et al. (2018) Lifestyle modifications: coordinating the tRNA epitranscriptome with codon bias to adapt translation during stress responses. Genome Biol 19:228

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