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Marianne Frommer : ウィキペディア英語版
Marianne Frommer

Marianne Frommer is an eminent Australian geneticist. She was born in Hong Kong and educated at the University of Sydney – BSc(Hons) 1969 and PhD in 1976. She is best known for developing a protocol to map DNA methylation by bisulphite genomic sequencing.
== Research ==
Early in her career Frommer investigated the molecular biology of "satellite DNAs" in the human genome. She and her colleague Jane Prosser showed that classical satellites were all A+T-rich simple repeated sequences.〔Frommer, M., Prosser, J., Tkachuk, D., Reisner, A.H. and Vincent, P.C. (1982). Simple repeated sequences in human satellite DNA. Nucl. Acids Res. 10: 547-563.
〕 Another important result was the identification of an Alu (SINE) sequence as part of the repeat unit in Satellite 1, thereby showing that SINEs could be a highly repeated component of centromeric heterochromatin.〔Frommer, M., Prosser, J. and Vincent, P.C. (1984). Human satellite I sequences include a male specific 2.47kb tandemly repeated unit containing one Alu family member per repeat. Nucl. Acids Res. 12: 2887-2900.〕
Frommer then determined the chromosomal locations of the major simple-sequence repeats by devising a new method of non-radioactive labelling, based on incorporation of bromodeoxyuridine into single-stranded probes.〔Frommer, M., Paul, C. and Vincent, P.C. (1988). Localisation of satellite DNA sequences on human metaphase chromosomes using bromodeoxyuridine-labelled probes. Chromosoma 97: 11-18.
〕 The method was used to localise satellite repeats very precisely. This research led to the observation of methylation patterns at CpG dinucleotides in sequenced genomic repeated DNA.
In 1984, Frommer was fortunate to spend a study leave in the laboratory of Dr Adrian Bird, and took part in the characterisation of what were then termed HTF (HpaII Tiny Fragments) islands in mammalian genomes.〔Bird, A., Taggart, M., Frommer, M., Miller, O.J. and Macleod, D. (1985). A fraction of the mouse genome that is derived from islands of nonmethylated, CpG-rich DNA. Cell 40: 91-99.〕 She and her PhD student Margaret Gardiner-Garden were able to identify these genomic components by DNA sequence characteristics alone, without prior knowledge of methylation status, and gave them the name "CpG islands.〔Gardiner-Garden, M. and Frommer, M. (1987). CpG islands in vertebrate genomes. J. Mol. Biol. 196: 261-282.〕 They showed that CpG islands are a distinct feature of vertebrate genomes and that CpG islands are associated with genes. They showed that the majority of neural and neuroendocrine genes were associated with CpG islands and therefore proposed that CpG islands facilitate regulated transcription from neural precursors and developing neural tissue in the early embryo.〔Gardiner-Garden, M. and Frommer, M. (1994). Transcripts and CpG islands associated with the pro-opiomelanocortin gene and other neurally expressed genes. J. Mol. Endocrinol. 12: 365-382.〕
In 1998 Frommer realised that it should be possible to amplify the products of a DNA deamination reaction and distinguish methylated and unmethylated molecules by dideoxy-sequencing.〔Frommer, M., McDonald, L.E., Millar, D.S., Collis, C.M., Watt, F., Grigg, G.W., Molloy, P.L. and Paul, C.L. (1992). A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands. Proc. Natl. Acad. Sci. USA 89: 1827-1831.〕 Frommer's protocol yielded a clear positive display of methylcytosine residues. The PCR products of bisulphite reactions could be sequenced directly to measure the extent of methylation at any CpG site in a population of DNA molecules. The particular strength of the method was that cloning and sequencing of the PCR products yielded methylation patterns or "maps" of single DNA molecules,.〔Clark, S.J., Harrison, J., Paul, C.L. and Frommer, M. (1994). High sensitivity mapping of methylated cytosines. Nucleic Acids Res. 22: 2990-2997.〕〔Clark, S.J., Statham, A., Stirzaker, C., Molloy, P.L. and Frommer, M. (2006). DNA methylation: Bisulphite modification and analysis. Nature Protocols 1: 2353-2364.〕
Frommer and her colleagues have also developed an extraordinarily powerful model system to study the molecular biology of behavioural characteristics and evolutionary processes using native Australian fruit flies,.〔An, X., Wilkes, K., Bastian, Y., Morrow, J.L., Frommer, M. and Raphael, K.A. (2002). The period gene in two species of tephritid fruit fly differentiated by mating behaviour. Insect Mol. Biol. 11: 419-430.〕〔Gilchrist, A.S., Shearman, D.C.A., Frommer, M., Raphael, K.A., Deshpande, N.P., Wilkins, M.R., Sherwin, W.B. and Sved, J.A. (submitted). The draft genome of the pest tephritid fruit fly Bactrocera tryoni: resources for the genomic analysis of hybridising species.〕

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