Abstract
Background: Mater is a maternal effect gene required for early embryonic development in mice, and its protein serves as an autoantigen in a mouse model of autoimmune premature ovarian failure. Methods: Human MATER cDNA was cloned by PCR techniques. The mRNA and protein were determined using hybridization and immunodetection respectively. The cDNA and protein sequences were analysed using bioinformatics software. Results: Human MATER gene spans a ∼63 kbp DNA at chromosome 19 and is composed of 15 exons and 14 introns. Expression of its mRNA (∼4.2 kb) is restricted to the oocytes. Human MATER cDNA (3885 nt) shows an open reading frame (3600 nt) encoding a polypeptide chain composed of 1200 residues with a predicted molecular mass of 134 236 Da. MATER protein (∼134 kDa) was detected in human oocytes. The human and mouse cDNA share 67% homology while their deduced polypeptide chains have 53% identity of amino acids. Also, their protein structures have a number of similar features. Conclusions: The human MATER and mouse Mater genes and proteins are conserved. Characterization of the human MATER and its protein provides a basis for investigating their clinical implications in autoimmune premature ovarian failure and infertility in women.
Author supplied keywords
Cite
CITATION STYLE
Tong, Z. B., Bondy, C. A., Zhou, J., & Nelson, L. M. (2002). A human homologue of mouse Mater, a maternal effect gene essential for early embryonic development. Human Reproduction, 17(4), 903–911. https://doi.org/10.1093/humrep/17.4.903
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.