Marilyn S. Kozak is an American professor of biochemistry at the Robert Wood Johnson Medical School. She was previously at the University of Medicine and Dentistry of New Jersey before the school was merged. She was awarded a PhD in microbiology by Johns Hopkins University studying the synthesis of the Bacteriophage MS2, advised by Daniel Nathans. ^{[1] [2]} In her original faculty job proposal, she sought to study the mechanism of eukaryotic translation initiation, a problem long thought to have already been solved by Joan Steitz. ^[3] While in the Department of Biological Sciences at University of Pittsburgh, she published a series of studies that established the scanning model of translation initiation and the Kozak consensus sequence. ^{[4] [5] [6]} Her current research interests are unknown as her last publication was in 2008. ^[7]

Recognition

Marilyn Kozak was listed as one of the top 10 Women Scientists of the 80's in an article published by The Scientist. This was awarded based on the number of citations for their published work between 1981-1988. During this time, Kozak had 3,107 citations. ^[4] Her most cited work was from 1984, entitled "Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs". ^[8] This paper highlighted the research that brought the known cellular mRNAs from 32 to 166.

Controversy

In March 2001, Kozak published a mini-review in the Journal of Molecular and Cellular Biology entitled "New Ways of Initiating Translation in Eukaryotes?" that resulted in push-back from the scientific community. ^[9] In her publication, Kozak discussed her hesitation towards the role of cellular internal ribosome entry sites (IRES). This was most heavily refuted by Robert Schneider, who published a response article of the same name in the same Journal in Dec. 2001. ^[10] In this response, Schneider claimed that in publishing her mini-review, Kozak hoped to increase the validity of her own findings. He further stated that Kozak's publication was not up to scholarly standards and should not have been accepted into the Journal of Molecular and Cellular Biology. ^[10] The existence of cellular IRESes remains controversial. ^{[11] [12] [13]}

Contributions

Along with her published work, Kozak has contributed to the scientific community with her role on the editorial board for the Journal of Molecular and Cellular Biology. She has been listed intermittently as an editor between the years 1983-1991. ^{[14] [15] [16]}

Selected works

This is a selection of Kozak's work but not a complete list.

• Kozak, M (October 1987). "An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs". Nucleic Acids Res. 15 (20): 8125–48. doi: 10.1093/nar/15.20.8125. PMC  306349. PMID  3313277. ^[5]
• Kozak, M (November 1991). "An analysis of vertebrate mRNA sequences: intimations of translational control". J. Cell Biol. 115 (4): 887–903. doi: 10.1083/jcb.115.4.887. PMC  2289952. PMID  1955461. ^[17]
• Kozak, M (1986). "Influences of mRNA secondary structure on initiation by eukaryotic ribosomes". Proc Natl Acad Sci U S A. 83 (9): 2850–4. Bibcode: 1986PNAS...83.2850K. doi: 10.1073/pnas.83.9.2850. PMC  323404. PMID  3458245. ^[18]
• Kozak, M. (1989). "The scanning model for translation: an update". The Journal of Cell Biology. 108 (2): 229–241. doi: 10.1083/jcb.108.2.229. PMC  2115416. PMID  2645293..
• Kozak, M (1987). "At least six nucleotides preceding the AUG initiator codon enhance translation in mammalian cells". J Mol Biol. 196 (4): 947–50. doi: 10.1016/0022-2836(87)90418-9. PMID  3681984. ^[19]
• Kozak, M (January 1986). "Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes". Cell. 44 (2): 283–92. doi: 10.1016/0092-8674(86)90762-2. PMID  3943125. S2CID  15613863. ^[20]
• Kozak, M (1981). "Possible role of flanking nucleotides in recognition of the AUG initiator codon by eukaryotic ribosomes". Nucleic Acids Res. 9 (20): 5233–52. doi: 10.1093/nar/9.20.5233. PMC  327517. PMID  7301588. ^[21]
• Kozak, M (2008). "Faulty old ideas about translational regulation paved the way for current confusion about how microRNAs function". Gene. 423 (2): 108–15. doi: 10.1016/j.gene.2008.07.013. PMID  18692553. ^[7]

References