Ming Gao
Assistant Professor
minggao@iun.edu
Marram Hall 310
219-980-6722
Office Hours:
By Appointment
Germ cells are essential for sexual reproduction and the survival of many species. Different species use different strategies to form germ cells. Drosophila melanogaster uses maternally inherited germ granules to determine germ cell fate. Germ granules are heterogeneous aggregates of ribonucleoprotein (RNP) complexes that undergo dynamic positional, morphological, and compositional changes during germline development, a process that spans oogenesis and early embryogenesis.
Me31B, a conserved germ granule component, is expressed in nurse cells, oocytes, and early embryos. In those cells, Me31B exists in different types of RNP granules, including nuage granules, P-bodies, sponge bodies, and germ plasm granules. In these granules, Me31B has been suggested to function as a putative ATP-dependent RNA helicase that interacts with other germline proteins and RNAs to exert post-transcriptional regulation on those RNAs. As an important example, Me31B associates with osk mRNA to ensure its proper translation into Osk protein only at the posterior pole of developing oocytes. Then, the Osk protein initiates a step-wise assembly pathway that recruits downstream proteins including Vas, Tud, and Aub to form the germ plasm and eventually dictates germ cell formation.
Me31B exhibits changes in its localization pattern, aggregation status, and even function as germline cells develop during the ovary-to-embryos transition. It is believed that these changes are correlated with the different biological contexts in which Me31B exists. We strive to understand the role and working mechanism of Me31B during germ cell development.
Our research is supported by:
IUN Research Project Initiation Grant to Ming Gao (Principle Investigator). Funded amount: $9,800.00 (2016 – 2017)