Insulin-dependent type 1A diabetes results from the autoimmune destruction
of pancreatic beta-cells. A targe body of evidence indicates that inherited
genetic factors influence both susceptibility and resistance to the diseas
e. At least 17 chromosomal regions have been linked to diabetes susceptibil
ity, suggesting that type 1A diabetes is a polygenic disorder. Alleles from
well-characterized susceptibility loci are commonly observed in the popula
tion and appear to have normal sequences. This suggests that susceptibility
may simply derive from polymorphisms affecting the function and expression
of certain proteins. There is also evidence for the existence of epistatic
phenomena involving several loci and of complex parental effects reportedl
y modifying the transmission and expression of inherited genes. Moreover, i
t is an intriguing but unproven possibility that additional genetic factors
or their expression may be acquired after birth, perhaps through environme
ntal exposures. Such factors may play a key role in triggering the process
leading to beta-cell destruction. This article summarizes the significant p
rogress made during the past few years in the identification of several sus
ceptibility loci and the understanding of the putative mechanisms by which
certain loci modulate susceptibility and resistance to type 1A diabetes. Fu
rther studies are expected to lead to the full identification and character
ization of susceptibility and perhaps disease genes. Such knowledge may imp
rove prediction by genetic testing and deepen our understanding of the key
mechanisms leading to the development of type 1A diabetes.