Abstract
The expression of mouse Peg3 (Paternally expressed gene 3) is driven by 4 promoters, including its main and three alternative promoters. The sexual, temporal and spatial specificity of these promoters was characterized in the current study. According to the results, the main promoter displays ubiquitous expression patterns throughout different stages and tissues. In contrast, the expression of Peg3 driven by the alternative promoter U2 was detected mainly in muscle and skin, but not in brain, starting from the late embryonic stage, revealing its tissue and stage specificity. The expression levels of both the main and U2 promoters are also sexually biased: the levels in females start higher but become lower than those in males during early postnatal stages. As an imprinted locus, the paternal alleles of these promoters are active whereas the maternal alleles are silent. Interestingly, deletion of the repressed maternal allele of the main promoter has an unusual effect on the opposite paternal allele, causing the up-regulation of both the main and U2 promoters. Overall, the promoters of Peg3 derive sexually biased and tissue-specific expression patterns.
Highlights
Peg3 (Paternally expressed gene 3) is an imprinted gene that is localized in human chromosome 19q13.4/mouse proximal chromosome 7 [1]
The results indicated that the main promoter is overall ubiquitous whereas the U2 promoter is stage and tissue-specific
The main and U2 promoters of Peg3 both are sexually biased in terms of their expression levels (Fig 2)
Summary
Peg (Paternally expressed gene 3) is an imprinted gene that is localized in human chromosome 19q13.4/mouse proximal chromosome 7 [1]. The mutations tend to have more severe effects on males than on females, suggesting the presence of potential sexual bias associated with the Peg locus [5,7,11,12]. This further suggests that the Peg locus may be subject to some unknown regulatory mechanisms other than genomic imprinting [12]
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.