DEVELOPMENTALLY-REGULATED EXPRESSION DURING GAMETOGENESIS OF THE MURINE GENE MEG1 SUGGESTS A ROLE IN MEIOSIS

Previous studies have shown that in adult male mice, expression of the meg1 gene is restricted to meiotic and early postmeiotic testicular g erm cells. We have now analyzed the expression of meg1 during postnata l testicular development and the comparable meiotic stages in the fema le. The 0.75 kb transcript for meg1 begins to accumulate in testes at d8-9 of postnatal (pn) development, coincident with the entry of germ cells into meiosis, and is expressed most abundantly at pn d14 and sub sequent stages, when the spermatocytes have entered pachytene. In situ hybridization analysis shows that meg1 is expressed at very low level s in leptotene cells and increases as the cells progress through zygot ene and pachytene stages. In the embryonic ovary, meg1 is not detected until after day 15 of gestation when the cells have entered the pachy tene stage of meiosis I. In situ hybridization analysis suggests that meg1 transcripts are expressed at higher levels in degenerating rather than in healthy pachytene stage oocytes; meg1 is not expressed in any cells of the adult ovary, regardless of the stage of follicular devel opment. These results suggest that meg1 is indeed a meiosis-associated gene in both male and female germ cells through the pachytene stage o f meiosis I and appears to exhibit sex-specific differences in its exp ression thereafter. (C) 1994 Wiley-Liss, Inc.