The eleven human pregnancy-specific glycoprotein (PSG) genes are tightly linked within
Ch 19q13.2. They are highly similar, have the same transcriptional orientation and are
essential for maintenance of gestation. PSG mRNAs and proteins are markedly induced
during trophoblast differentiation. However, little is known about the transcriptional
control and expression pattern of each PSG gene. Objectives: This report examines
the expression level and transcriptional activation of five PSG genes during in vitro syncytialization
of human trophoblast cells. Methods:
Jeg3 cells were induced to differentiate into syncytium- like structures. RNA isolated
at different times was analyzed by semi-quantitative RT-PCR using PSG transcript specific
primers. Transient transfection assays of PSG promoters:LUC constructs were performed.
Results: PSG expression of all analyzed transcripts increased during
differentiation. PSG3, 5 and 7 promoter constructs bearing up to 600 pb of the 5 ´ proximal
regulatory region revealed different basal promoter activities which were increased upon
differentiation. In addition, treatment of Jeg3 cells with chromatin modifying reagents induced
increased transcription of endogenous PSG genes. Conclusions: Our results suggest
that transcription of all PSG family members are activated during trophoblast
differentiation. This activation involves regulatory elements present within the 5 ´ proximal
regulatory region, as well as, chromatin modifications. Supported by CONICET,
FONCYT and SECyT UNC.