Lipoprotein lipase (LPL) serves as a central factor in hydrolysis of triacylglycerol and uptake of free fatty acids from the plasma. However, there are limited data concerning the action of
LPL on the regulation of milk fat synthesis in goat mammary gland. In this investigation, we describe the cloning and sequencing of the
LPL gene from Xinong Saanen dairy goat mammary gland, along with a study of its phylogenetic relationships. Sequence analysis showed that goat
LPL shares similarities with other species including sheep, bovine, human and mouse.
LPL mRNA expression in various tissues determined by RT-qPCR revealed the highest expression in white adipose tissue, with lower expression in heart, lung, spleen, rumen, small intestine, mammary gland, and kidney. Expression was almost undetectable in liver and muscle. The expression profiles of
LPL gene in mammary gland at early, peak, mid, late lactation, and the dry period were also measured. Compared with the dry period,
LPL mRNA expression was markedly greater at early lactation. However, compared with early lactation, the expression was lower at peak lactation and mid lactation. Despite those differences,
LPL mRNA expression was still greater at peak, mid, and late lactation compared with the dry period. Using goat mammary epithelial cells (GMEC), the
in vitro knockdown of
LPL via shRNA or with Orlistat resulted in a similar degree of down-regulation of
LPL (respectively). Furthermore, knockdown of
LPL was associated with reduced mRNA expression of
SREBF1,
FASN,
LIPE and
PPARG but greater expression of
FFAR3. There was no effect on
ACACA expression. Orlistat decreased expression of
LIPE,
FASN,
ACACA, and
PPARG, and increased
FFAR3 and
SREBF1 expression. The pattern of
LPL expression was similar to the changes in milk fat percentage in lactating goats. Taken together, results suggest that
LPL may play a crucial role in fatty acid synthesis.
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