Polyunsaturated fatty acids (PUFAs), specifically the n-3 and n-6 series, p
lay a key role in the progression or prevention of human diseases such as o
besity, diabetes, cancer, neurological and heart disease, mainly by affecti
ng cellular membrane lipid composition, metabolism, signal-transduction pat
hways, and by direct control of gene expression. PUFAs show regulation of g
ene expression in several tissues, including brain, liver, heart, and adipo
se. Most recently, research has focused on identifying the mechanisms by wh
ich PUFAs regulate lipogenic gene expression. Research to date indicates th
at PUFA-mediated regulation of the genetic expression and proteolytic matur
ation of a group of transcription factors termed sterol regulatory element
binding proteins (SREBPs) accounts for the suppression of hepatic lipogenic
gene expression. However, our recent studies on the transcriptional regula
tion of the stearoyl-coenzyme A (CoA) desaturase gene, encoding a key enzym
e in the cellular synthesis of monounsaturated fatty acids from saturated f
atty acids indicates that PUFA can suppress gene transcription by a mechani
sm independent of SREBP maturation.