Mon 2:00 pm – 3:00 pm; Wed 5:00 pm – 6:00 pm. Or by appointment
Molecular developmental biology. Regulation of gene expression by RNA translational control and its role in cell cycle progression during oocyte maturation, maternal to embryo transition, and early development.
B.Sc. Biochemistry, University of Kent at Canterbury, UK (1992)
Ph.D. Cell Biology, University College London, UK (1996)
I have a background in signal transduction and cell cycle regulation in the fields of neurobiology, cancer biology and developmental biology, using biochemical, molecular biology and cell biology approaches. These experiences were acquired in large pharmaceutical companies, medical research institutes, medical schools and undergraduate universities.
My current research focuses on gene expression in early development. After fertilization the male genome is not used immediately. Instead, important developmental process are controlled by mRNAs that were pre-loaded into the egg by the female. Important questions that we don't know the answers to are how are these mRNAs used at the right time, in the right place.
The mRNAs that are donated by the female contain instructions that control the time of their activation. My lab is identifying and characterising these instructions. We are also identifying and characterising the factors that decode these instructions.
Student researchers gain experience and expertise in cell and molecular biology methods including protein analysis, cloning, cell based luciferase reporter assays, and RT-PCR-based RNA analysis.
15 out of 27
2017 Cook, J. M., and Charlesworth, A. (2017) Insertion of inter-domain linkers improves expression and bioactivity of Zygote arrest (Zar) fusion proteins. Prot. Eng. Des. Sel. doi: 10.1093/protein/gzx002 Pubmed
2013 Yamamoto, T., Cook, J. M., Kotter, C. V., Khat, T., Silva, K. D., Ferreyros, M, Holt, J. W., Knight, J. D., and Charlesworth, A. (2013) Zar1 represses translation in Xenopus oocytes and binds to the TCS in maternal mRNAs with different characteristics than Zar2. Biochimica et biophysica acta, 1829: 1034-1046. PubMed
2013 Charlesworth, A., Meijer, H.A., and de Moor, C.H. (2013) Specificity factors in cytoplasmic polyadenylation. (2013) WIREs RNA, 4: 437-461 (Invited Review) PubMed
2012 Charlesworth A, Yamamoto TM, Cook JM, Silva KD, Kotter CV, Carter GS, Holt JW, Lavender HF, MacNicol AM, Wang YY, Wilczynska A. (2012) Xenopus laevis Zygote arrest 2 (zar2) encodes a zinc finger RNA-binding protein that binds to the Translational Control Sequence in the maternal Wee1 mRNA and regulates translation. Dev. Bio., 369:177-190 PubMed
2008 Wang, Y., Charlesworth, A., Byrd, S.M., Gregerson, R., MacNicol, M.C., MacNicol, A.M. (2008) A novel mRNA 3' untranslated region translational control sequence regulates Xenopus Wee1 mRNA translation. Dev. Bio., 317: 454-466 PubMed
2006 Charlesworth, A., Wilczynska, A., Thampi, P., Cox, L.L. and MacNicol, A.M. (2006) Musashi regulates the temporal order of mRNA translation during Xenopus oocyte maturation. EMBO J., 25: 2792-2801 PubMed
2004 Charlesworth A., Cox L. L. and MacNicol A.M. (2004) Cytoplasmic Polyadenylation Element (CPE)- and CPE-binding Protein (CPEB)-independent Mechanisms Regulate Early Class Maternal mRNA Translational Activation in Xenopus Oocytes. J. Biol. Chem. 279: 17650-17659 PubMed
2002 Charlesworth A., Ridge J.A., King L.A., MacNicol M.C. and MacNicol A.M. (2002) A novel regulatory element determines the timing of Mos mRNA translation during Xenopus oocyte maturation. EMBO J., 21: 2798-2806. PubMed
2001 Welk J.F., Charlesworth A. and MacNicol A.M. (2001) Identification and characterization of a human cytoplasmic polyadenylation element binding protein. Gene, 263: 113-120. PubMed
2000 Charlesworth A., Welk J. and MacNicol A.M. (2000) The temporal control of Wee1 mRNA translation during Xenopus oocyte maturation is regulated by cytoplasmic polyadenylation elements within the 3’ untranslated region. Dev. Bio., 227: 706-719. PubMed
1999 Howard E.L., Charlesworth A., Welk J. and MacNicol A.M. (1999) The MAP kinase signaling pathway stimulates Mos mRNA cytoplasmic polyadenylation during Xenopus oocyte maturation. Mol. Cell. Biol., 19: 1990-1999. PubMed
1997 Charlesworth A. and Rozengurt E. (1997) Bombesin and neuromedin B stimulate the activation of p42mapk and p74raf-1 via a PKC-independent pathway in Rat-1 cells. Oncogene, 14: 2323 – 2329. PubMed
1996 Charlesworth A., Broad S. and Rozengurt E. (1996) The bombesin/GRP receptor transfected into Rat-1 fibroblasts couples to phospholipase C activation, tyrosine phosphorylation of p125FAK and paxillin and cell proliferation. Oncogene, 12: 1337-1345. PubMed
1994 Charlesworth A. and Rozengurt E. (1994) Thapsigargin and di-tert-butylhydroquinone induce synergistic stimulation of DNA synthesis with phorbol ester and bombesin in Swiss 3T3 cells. J. Biol. Chem., 269: 32528 – 32535. PubMed
1992 McAllister G., Charlesworth A., Snodin C., Beer M.S., Noble A.J., Middlemiss D.N., Iversen L.L. and Whiting P. (1992) Molecular cloning of a serotonin receptor from human brain (5HT1E): A fifth 5HT1-like subtype. Proc. Natl. Acad. Sci., USA 89: 5517- 5521. PubMed
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