Marco Conti, MD

Professor
Department of Obstetrics Gynecology & Reproductive Sciences
Center for Reproductive Sciences
Research Overview: 

Dr. Conti's research focuses on signal transduction required for germ cell development. Over the past 15 years, we have charted signaling pathways controlling oocyte meiotic maturation and competence for development into an embryo. We have identified critical signals arising in the somatic cells at the time of ovulation that are required to establish oocyte developmental competence. Genetic models that disrupt these pathways and compromise developmental competence and early embryo development have been established.

Focus of the experiments is on understanding how disruption of developmental competence in these genetic models is reflected in the pattern of recruitment of maternal mRNA translation into proteins critical for nuclear reprogramming and early embryo development. This strategy has the potential to identify components critical for the epigenetic regulations required for early embryo development. The impact of this research program on stem cell research is twofold. These studies are relevant to the understanding of the mechanisms controlling cell replication and nuclear reprogramming during preimplantation embryo development and lineage specification.

A better understanding of the biochemical mechanisms controlling oocyte maturation is essential for successful development of embryonic stem cells into artificial gametes. In addition, they will provide insights into mechanisms necessary for successful somatic nuclear transfer critical to the derivation of hESC for therapeutic use.

Primary Thematic Area: 
Developmental & Stem Cell Biology
Secondary Thematic Area: 
None
Research Summary: 
Mechanisms of Action of Peptide Hormones and Growth Factors
Publications: 

Phosphodiesterases 4B and 4D Differentially Regulate cAMP Signaling in Calcium Handling Microdomains of Mouse Hearts.

Cells

Kraft AE, Bork NI, Subramanian H, Pavlaki N, Failla AV, Zobiak B, Conti M, Nikolaev VO

Multiple intersecting pathways are involved in the phosphorylation of CPEB1 to activate translation during mouse oocyte meiosis.

bioRxiv : the preprint server for biology

Kunitomi C, Romero M, Daldello EM, Schindler K, Conti M

A genome-wide perspective of the maternal mRNA translation program during oocyte development.

Seminars in cell & developmental biology

Conti M, Kunitomi C

Author Correction: CPEB1-dependent disruption of the mRNA translation program in oocytes during maternal aging.

Nature communications

Takahashi N, Franciosi F, Daldello EM, Luong XG, Althoff P, Wang X, Conti M