Sarah Elgin

Sarah Elgin
Sarah C.R. Elgin

Sarah C.R. Elgin
Residence St. Louis, MO
Nationality American
Fields Biochemistry, Biophysics, Genetics, Epigenetics
Institutions California Institute of Technology; Harvard University; Washington University in St. Louis
Alma mater Pomona College, California Institute of Technology
Doctoral advisor James Bonner
Doctoral students Tharappel C James, Lee M. Silver, Carl Wu [1]
Other notable students Joel Eissenberg [2], David S. Gilmour [3], Lori L. Wallrath [4]
Known for heterochromatin, science education
Notable awards
  • Fellows Award, Academy of Science of St. Louis
  • Faculty Award, Council of Students of Arts and Sciences, WU
  • Missouri Governor's Award for Excellence in Teaching
  • Award for Exemplary Contributions to Education, ASBMB
  • Bruce Alberts Award for Excellence in Science Education, ASCB
  • Elizabeth W. Jones Award for Excellence in Education, GSA

Sarah C.R. Elgin is an American biologist noted for her work in epigenetics, gene regulation, and heterochromatin and her contributions to science education.

In high school, Elgin studied fallout levels in Oregon rainwater after nuclear weapons tests in the Soviet Union. She received her B.A. in chemistry from Pomona College. While at Pomona, she participated in a summer research program at the University of Leeds characterizing the egg stalk of the green lacewing fly Chrysopa vittata.[1] Elgin did her graduate work in the lab of James Bonner at the California Institute of Technology, isolating and characterizing nonhistone chromosomal proteins from rat livers. She received her Ph.D. in biochemistry in 1972. Elgin stayed at Caltech for her postdoctoral research, working in the lab of Leroy Hood. She continued to isolate and characterize nonhistone chromosomal proteins but started studying Drosophila.

After her postdoc, Elgin joined the faculty at Harvard University, where her lab pioneered immunostaining of polytene chromosomes from Drosophila larval salivary glands[2] and nuclease digestion assays.[3][4]

In 1981, Elgin joined the faculty in the Department of Biology at Washington University in St. Louis. Her lab isolated and characterized Heterochromatin Protein 1 in Drosophila[5] (now known as Su(var)205 or HP1a). To probe chromatin environments, her lab developed a P element construct with a copy of the white gene driven by the hsp70 promoter. When this reporter gene is inserted into heterochromatic environments, the fly eyes display a vareigating phenotype, whereas when the P element is inserted into euchromatin the fly eyes show a red phenotype; this phenomenon is known as Position-effect variegation. Nuclease digestion assays have confirmed that the eye phenotypes are indicative of the chromatin environment surrounding the P element insertion site.[6][7] In 2006, Elgin was named as the inaugural Viktor Hamburger Distinguished Professor in Arts and Sciences [5].


At Washington University and in the St. Louis area, Elgin has been active in science education. She founded the Washington University Science Outreach program in 1989 [6] and has been active in science education in the University City school district.

Sarah Elgin examines flies in lab, 2003
Examining Flies

In 2002 Elgin became an HHMI Professor [7][8] with the goal to develop core curriculum to integrate primary research in genomics with a college course. This project has been expanded and disseminated as the Genomics Education Partnership [9], a consortium of 66 member colleges and universities [10] who participate in sequence improvement and annotation projects with the goal of publishing the results in primary research journals.[8][9]

Memberships

Notes and references

  1. ^ Roberts, S.C. (1966). "Brief description of the early stages of Chrysopa vittata (Neuroptera Chrysopidae)". Entomologist's Gazette 17: 85–89. 
  2. ^ Silver, L M; S C Elgin (1976 February). "A method for determination of the in situ distribution of chromosomal proteins". Proc Natl Acad Sci U S A 73 (2): 423–427. doi:10.1073/pnas.73.2.423. PMC 335921. PMID 813226. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=335921. 
  3. ^ Wu, C; PM Bingham, KJ Livak, R Holmgren, and SCR Elgin (1979 April). "The chromatin structure of specific genes: I. Evidence for higher order domains of defined DNA sequence". Cell 16 (4): 797–806. doi:10.1016/0092-8674(79)90095-3. PMID 455449. http://www.sciencedirect.com/science/article/pii/0092867479900953. 
  4. ^ Wu, C; YC Wong, SCR Elgin (1979 April). "The chromatin structure of specific genes: II. Disruption of chromatin structure during gene activity". Cell 16 (4): 807–814. doi:10.1016/0092-8674(79)90096-5. PMID 455450. http://www.sciencedirect.com/science/article/pii/0092867479900965. 
  5. ^ James, TC; SCR Elgin (1986 Nov). "Identification of a nonhistone chromosomal protein associated with heterochromatin in Drosophila melanogaster and its gene". Mol Cell Biol 6 (11): 3862–3872. PMC 367149. PMID 3099166. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=367149. 
  6. ^ Wallrath, LL; SCR Elgin (1995-05-15). "Position effect variegation in Drosophila is associated with an altered chromatin structure". Genes & Develop 9 (10): 1263–1277. doi:10.1101/gad.9.10.1263. PMID 7758950. 
  7. ^ Sun, FL; MH Cuaycong, SCR Elgin (2001 April). "Long-Range Nucleosome Ordering Is Associated with Gene Silencing in Drosophila melanogaster Pericentric Heterochromatin". Mol Cell Biol 21 (8): 2867–2879. doi:10.1128/MCB.21.8.2867-2879.2001. PMC 86916. PMID 11283265. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=86916. 
  8. ^ Slawson, EE; Shaffer CD, Malone CD, Leung W, Kellmann E, Shevchek RB, Craig CA, Bloom SM, Bogenpohl J 2nd, Dee J, Morimoto ET, Myoung J, Nett AS, Ozsolak F, Tittiger ME, Zeug A, Pardue ML, Buhler J, Mardis ER, Elgin SC (2006-02-20). "Comparison of dot chromosome sequences from D. melanogaster and D. virilis reveals an enrichment of DNA transposon sequences in heterochromatic domains". Genome Biol 7 (2): R15. doi:10.1186/gb-2006-7-2-r15. PMID 16507169. http://genomebiology.com/content/7/2/R15. 
  9. ^ Leung, W; Shaffer CD, Cordonnier T, Wong J, Itano MS, Slawson Tempel EE, Kellmann E, Desruisseau DM, Cain C, Carrasquillo R, Chusak TM, Falkowska K, Grim KD, Guan R, Honeybourne J, Khan S, Lo L, McGaha R, Plunkett J, Richner JM, Richt R, Sabin L, Shah A, Sharma A, Singhal S, Song F, Swope C, Wilen CB, Buhler J, Mardis ER, Elgin SC (2010 Aug). "Evolution of a distinct genomic domain in Drosophila: comparative analysis of the dot chromosome in Drosophila melanogaster and Drosophila virilis". Genetics 185 (4): 1519–1534. doi:10.1534/genetics.110.116129. PMID 20479145. http://www.genetics.org/content/185/4/1519.long. 

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