Mary Lyon: A Tribute.
Mary Lyon: A Tribute.
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玛丽·里昂:致敬。
DOI:
10.1016/j.ajhg.2015.09.002
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发表时间:
2015
影响因子:
9.8
通讯作者:
Mueller,JacobL
中科院分区:
文献类型:
--
作者:
Kalantry,Sundeep;Mueller,JacobL
Mary Lyon passed away on Christmas Day, 2014, at the age of 89. Best known for the X-chromosome-inactivation hypothesis, Mary Lyon was a pioneering geneticist whose findings and syntheses have left a lasting imprint on our understanding of mammalian development and disease (Figure 1). She was the recipient of the 1986 William Allan Award, 1 the most prestigious prize given by the American Society of Human Genetics.Mary Lyon was born in 1925 in Norwich, England. Her interest in biology arose while she was a secondary school student at King Edward VII School in Birmingham. Later, despite difficulties posed as a result of air raids and a scarcity of specialist teachers during World War II, Lyon passed the University of Cambridge entrance examination and entered Girton College at Cambridge. Lyon’s admission into Cambridge was all the more impressive because at the time, women constituted only~ 10% of the entire student populace. At Cambridge, Lyon studied zoology and graduated in 1946 with a ‘‘titular’’degree, given that women were not considered official members of the university then (in 1998, in a special ceremony, Cambridge awarded her a BA). It was as a student at Cambridge that Lyon became intrigued by genetic regulation as the basis of embryonic development. Lyon worked with RA Fisher, a professor of genetics at Cambridge University and cofounder of the field of population genetics, to pursue a Ph. D. in the growing discipline of mouse genetics. Finding her experience there unsatisfactory, Lyon transferred to the University of Edinburgh and joined the Institute of Animal Genetics, headed by the eminent embryologist Conrad H. Waddington. After completing her Ph. D. in Edinburgh with Douglas Falconer in 1950, she stayed on to work in Toby Carter’s group to investigate the heritable mutagenic effects of radiation through mice. In search of more mouse space, in 1954 Carter moved his group to the Medical Research Council (MRC)-funded Radiobiology Unit at Harwell. Although Lyon’s studies on mutations induced by radiation in mice garnered much interest, her studies in developmental genetics were what had a lasting impact. The abundance of radiation-induced and spontaneously arising mouse mutants at MRC Harwell dovetailed with Lyon’s interest in developmental genetics. In fact, one such mutant strain, mottled, 2 was instrumental in Lyon’s formulation of the X-inactivation hypothesis. 3 The mottled mutant phenotype, paradoxically, arose in a male. Whereas some cells in the mottled male carried the
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DOI:
--
发表时间:
2004
期刊:
Zeitschrift für Vererbungslehre
影响因子:
--
作者:
B. Cattanach
通讯作者:
B. Cattanach
DOI:
--
发表时间:
1950
影响因子:
11.1
作者:
L. C. Dunn;S. Gluecksohn‐Schoenheimer
通讯作者:
S. Gluecksohn‐Schoenheimer
DOI:
--
发表时间:
1956
期刊:
影响因子:
--
作者:
M. Lyon
通讯作者:
M. Lyon
影响因子:
3.8
作者:
M. Lyon;R. Meredith
通讯作者:
R. Meredith
DOI:
--
发表时间:
1959
影响因子:
11.1
作者:
W. Welshons;L. B. Russell
通讯作者:
L. B. Russell