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Jack D. Keene

August 31, 2023

Jack D. Keene (born June 22, 1947, Jacksonville, Florida) is a James B. Duke Professor of Molecular Genetics and Microbiology at Duke University.[1]

Jack Donald Keene
Born
Jack Donald Keene

(1947-06-22)June 22, 1947
Jacksonville, Florida
Alma materUniversity of California, Riverside, University of Washington
Scientific career
InstitutionsDuke University

Keene studies the regulation of RNA and the mechanisms of RNA-protein interactions.[2][3] He identified RNA recognition motif (RRM) proteins, which are the largest family of RNA-binding proteins. He isolated the first human autoimmune antigen. He formalized the posttranscriptional operon and regulon (PTRO) model to describe global gene regulation, and proposed the RNA regulon hypothesis to better understand post-transcriptional regulation of mRNAs encoding proteins.[3][4] Keene introduced the RIP (ribonucleoprotein immunoprecipitation) protocol for isolating specific mRNPs, which has become a tool for the mapping of mRNA targets of specific RBPs.[5]

Early life and education Edit

Jack Donald Keene was born in Jacksonville, Florida on June 22, 1947. His father worked for the RAND Corporation.[6][7] Keene attended Redlands High School in Redlands, California, graduating in 1965.[1]

Initially a student at University of California, Los Angeles (UCLA), he transferred to the University of California, Riverside, where he majored in biology, working with Carlton Bovell.[6] He received his A.B. degree in 1969.[7] Next, Keene studied with Helen Riaboff Whiteley at the University of Washington in Seattle, Washington, graduating in 1975 with a doctorate in microbiology and Immunology.[1][6]

He did postdoctoral work in molecular virology with Robert A. Lazzarini in the Laboratory for Molecular Genetics at the National Institutes of Health in Bethesda, Maryland from 1974 to 1978.[3][1][6][7]

Career Edit

In 1979, Keene was recruited by Wolfgang Joklik to the department of microbiology and immunology at Duke University Medical Center. At that time the department was ranked one of the top three in the United States by the National Research Council.[3] Keene was the chairman of the department of microbiology from 1992 to 2002,[3] and director of basic sciences for the Duke Comprehensive Cancer Center from 1995 to 2003.[7] As of 1997 he became the James B. Duke Professor of Molecular Genetics and Microbiology at Duke University.[8] In 1999 Keene founded the Duke Center for RNA Biology.[1]

Research Edit

Keene studies the regulation of RNA and the mechanisms of RNA-protein interactions.[2][9][10]

In his work on molecular genetics, he and his coworkers have examined the role of DNA and RNA-binding proteins (RBPs) in the pathogenesis of autoimmunity.[3] In the late 1970s and early 1980s he identified genomic sequences for vesicular stomatitis virus (VSV) and rabies virus (RABV), members of the Rhabdoviridae family of viruses,[11][12] and for Ebola virus and Marburg virus from the broader group of negative-strand RNA viruses (NSRV).[13][14] He identified the origins of defective interfering particles of negative-strand RNA viruses.[15] Through combinatorial studies of viral and bacterial systems, he has identified targets for novel pharmacological studies.[3]

Later in the 1980s, Keene identified RNA recognition motif (RRM) proteins. RRM proteins are the largest family of RNA-binding proteins and the seventh largest protein family of the human genome. RRM is a prevalent RNA-binding fold involving proteins implicated in RNA biogenesis, processing, transport, and degradation.[3][16]

In 1987, Query and Keene first identified a B-cell epitope within the U1-70K protein.[17][18] Keene isolated the first human autoimmune antigen and elucidated its autoimmune epitopes, the parts of an antigen to which antibodies in the immune system can bind.[3] He cloned rheumatological autoimmune protein genes. He developed a diagnostic test for systemic lupus erythematosus using recombinant antigens.[3][19][20]

Keene's lab has identified functions of the ELAV/Hu posttranscriptional regulators HuB, HuC and HuD and their roles and that of HuR in processes of growth, proliferation, differentiation, and immune response.[3][21][22][23] The study of RNA-binding proteins such as HuR and the determination of the binding of specific sequences have informed Keene's later post-transcription theory and his coordination theory of RNA operons.[6][3]

RNA-binding proteins appear to be implicated in the functioning of many posttranscriptional processes. As of 1994, Keene suggested that RNA-binding proteins could be involved in the regulation of messenger RNA that encode cytokines. In 2000, he was able to apply this approach to demonstrate neuronal differentiation.[1] He also introduced the first use of the RIP (ribonucleoprotein immunoprecipitation) protocol, isolating specific mRNPs using immunoprecipitation, and identifying the mRNA component with microarray or deep sequencing. This method has become a tool for the mapping of mRNA targets of specific RBPs.[5][24]

In 2001–2002, Keene formalized the posttranscriptional operon and regulon (PTRO) model for global gene regulation.[3][25][26] By 2007, Keene proposed the RNA regulon hypothesis, "that mRNAs encoded by functionally related genes may be coordinately regulated as posttranscriptional RNA regulons by specific mRNP processing machineries".[27] The purpose of the RNA regulon model was to better understand post-transcriptional regulation, to answer the question "How does the cell coordinate metabolism and regulation of mRNAs encoding proteins in the same biological process so that the proteins can be coordinately produced?"[4][28][29]

Awards and honors Edit

References Edit

  1. ^ a b c d e f "Jack Keene, PhD – Biography". Duke University. Retrieved 5 November 2019.
  2. ^ a b Doyle, Francis; Tenenbaum, Scott A. (15 April 2014). "Trans-regulation of RNA-binding protein motifs by microRNA". Frontiers in Genetics. 5: 79. doi:10.3389/fgene.2014.00079. PMC 4006066. PMID 24795744.
  3. ^ a b c d e f g h i j k l m Hamilton, John D. (February 10, 2015). The History of Infectious Diseases At Duke University In the Twentieth Century. Lulu Publishing Services. pp. 139–140. ISBN 9781483423753. Retrieved 23 February 2020.
  4. ^ a b Culjkovic-Kraljacic, Biljana; Borden, Katherine L. B. (5 November 2018). "The Impact of Post-transcriptional Control: Better Living Through RNA Regulons". Frontiers in Genetics. 9: 512. doi:10.3389/fgene.2018.00512. PMC 6230556. PMID 30455716.
  5. ^ a b Sanford, Jeremy R.; Penalva, Luiz O. F. (29 November 2017). "The 3′ end of the story: deciphering combinatorial interactions that control mRNA fate". Genome Biology. 18 (1): 227. doi:10.1186/s13059-017-1360-6. PMC 5707901. PMID 29187223.
  6. ^ a b c d e f g h Center for Oral History. "Jack D. Keene". Science History Institute.
  7. ^ a b c d Thackray, Arnold; Morris, Stephanie; Caruso, David (2008). Jack D. Keene, Transcript of an Interview Conducted by Arnold Thackray, Stephanie Morris, and David Caruso at Ixtapa, Mexico, and Johns Hopkins University, Baltimore, Maryland on 5 March 1989 and 23 and 25 April 2008. Philadelphia, PA: Chemical Heritage Foundation.
  8. ^ "Jack Donald Keene". Scholars @ Duke University. Retrieved 8 February 2020.
  9. ^ Keene, J. D. (January 2007). "Biological Clocks and the Coordination Theory of RNA Operons and Regulons". Cold Spring Harbor Symposia on Quantitative Biology. 72 (1): 157–165. doi:10.1101/sqb.2007.72.013. PMID 18419273.
  10. ^ Keene, Jack D. (April 2010). "Minireview: Global Regulation and Dynamics of Ribonucleic Acid". Endocrinology. 151 (4): 1391–1397. doi:10.1210/en.2009-1250. PMC 2850242. PMID 20332203.
  11. ^ Wagner, Robert R. (June 29, 2013). The Rhabdoviruses. Springer Science & Business Media. pp. 139–140. ISBN 9781468470321.
  12. ^ Keene, J. D.; Schubert, M.; Lazzarini, R. A.; Rosenberg, M. (1 July 1978). "Nucleotide sequence homology at the 3' termini of RNA from vesicular stomatitis virus and its defective interfering particles". Proceedings of the National Academy of Sciences. 75 (7): 3225–3229. Bibcode:1978PNAS...75.3225K. doi:10.1073/pnas.75.7.3225. PMC 392747. PMID 210454.
  13. ^ Deflubé, Laure R.; Cressey, Tessa N.; Hume, Adam J.; Olejnik, Judith; Haddock, Elaine; Feldmann, Friederike; Ebihara, Hideki; Fearns, Rachel; Mühlberger, Elke (23 April 2019). "Ebolavirus polymerase uses an unconventional genome replication mechanism". Proceedings of the National Academy of Sciences. 116 (17): 8535–8543. doi:10.1073/pnas.1815745116. PMC 6486738. PMID 30962389.
  14. ^ Kiley, Michael P.; Wilusz, Jeffrey; Mc Cormick, Joseph B.; Keene, Jack D. (March 1986). "Conservation of the 3′ terminal nucleotide sequences of Ebola and Marburg virus". Virology. 149 (2): 251–254. doi:10.1016/0042-6822(86)90127-3. PMID 3946083.
  15. ^ Lazzarini, Robert A.; Keene, Jack D.; Schubert, Manfred (October 1981). "The origins of defective interfering particles of the negative-strand RNA viruses". Cell. 26 (2): 145–154. doi:10.1016/0092-8674(81)90298-1. PMID 7037195.
  16. ^ Loerch, Sarah; Kielkopf, Clara L. (September 2015). "Dividing and Conquering the Family of RNA Recognition Motifs: A Representative Case Based on hnRNP L". Journal of Molecular Biology. 427 (19): 2997–3000. doi:10.1016/j.jmb.2015.06.009. PMC 4820351. PMID 26101840.
  17. ^ Kattah, Nicole H.; Kattah, Michael G.; Utz, Paul J. (January 2010). "The U1-snRNP complex: structural properties relating to autoimmune pathogenesis in rheumatic diseases". Immunological Reviews. 233 (1): 126–145. doi:10.1111/j.0105-2896.2009.00863.x. PMC 3074261. PMID 20192997.
  18. ^ Query, C (October 1987). "A human autoimmune protein associated with U1 RNA contains a region of homology that is cross-reactive with retroviral p30gag antigen". Cell. 51 (2): 211–220. doi:10.1016/0092-8674(87)90148-6. PMC 3074261. PMID 2959371.
  19. ^ Habets, WJ; Hoet, MH; Sillekens, PT; De Rooij, DJ; Van de Putte, LB; Van Venrooij, WJ (May 1989). "Detection of autoantibodies in a quantitative immunoassay using recombinant ribonucleoprotein antigens". Clinical and Experimental Immunology. 76 (2): 172–7. PMC 1541836. PMID 2527098.
  20. ^ Chambers, J. C.; Keene, J. D. (1 April 1985). "Isolation and analysis of cDNA clones expressing human lupus La antigen". Proceedings of the National Academy of Sciences. 82 (7): 2115–2119. Bibcode:1985PNAS...82.2115C. doi:10.1073/pnas.82.7.2115. PMC 397503. PMID 3856888.
  21. ^ Simone, Laura E; Keene, Jack D (February 2013). "Mechanisms coordinating ELAV/Hu mRNA regulons". Current Opinion in Genetics & Development. 23 (1): 35–43. doi:10.1016/j.gde.2012.12.006. PMC 3617084. PMID 23312841.
  22. ^ Bevilacqua, Annamaria; Ceriani, Maria Cristina; Capaccioli, Sergio; Nicolin, Angelo (June 2003). "Post-transcriptional regulation of gene expression by degradation of messenger RNAs". Journal of Cellular Physiology. 195 (3): 356–372. doi:10.1002/jcp.10272. PMID 12704645.
  23. ^ Mansfield, Kyle D.; Keene, Jack D. (March 2012). "Neuron-specific ELAV/Hu proteins suppress HuR mRNA during neuronal differentiation by alternative polyadenylation". Nucleic Acids Research. 40 (6): 2734–2746. doi:10.1093/nar/gkr1114. PMC 3315332. PMID 22139917.
  24. ^ Keene, J. D. (19 June 2001). "Ribonucleoprotein infrastructure regulating the flow of genetic information between the genome and the proteome". Proceedings of the National Academy of Sciences. 98 (13): 7018–7024. Bibcode:2001PNAS...98.7018K. doi:10.1073/pnas.111145598. PMC 34616. PMID 11416181.
  25. ^ Aparicio, Luis A.; Abella, Vanessa; Valladares, Manuel; Figueroa, Angélica (29 May 2013). "Posttranscriptional regulation by RNA-binding proteins during epithelial-to-mesenchymal transition". Cellular and Molecular Life Sciences. 70 (23): 4463–4477. doi:10.1007/s00018-013-1379-0. PMC 3827902. PMID 23715860.
  26. ^ Keene, Jack D. (July 2007). "RNA regulons: coordination of post-transcriptional events" (PDF). Nature Reviews Genetics. 8 (7): 533–543. doi:10.1038/nrg2111. PMID 17572691. Retrieved 8 February 2020.
  27. ^ Wang, Li; Miao, Yi-Liang; Zheng, Xiaofeng; Lackford, Brad; Zhou, Bingying; Han, Leng; Yao, Chengguo; Ward, James M.; Burkholder, Adam; Lipchina, Inna; Fargo, David C.; Hochedlinger, Konrad; Shi, Yongsheng; Williams, Carmen J.; Hu, Guang (December 2013). "The THO Complex Regulates Pluripotency Gene mRNA Export and Controls Embryonic Stem Cell Self-Renewal and Somatic Cell Reprogramming". Cell Stem Cell. 13 (6): 676–690. doi:10.1016/j.stem.2013.10.008. PMC 3962795. PMID 24315442.
  28. ^ Pulendran, Bali; Katsikis, Peter D.; Schoenberger, Stephen P., eds. (August 19, 2011). Crossroads between Innate and Adaptive Immunity III. Springer Science & Business Media. pp. 1–3. ISBN 9781441956323. Retrieved 24 February 2020.
  29. ^ Larsson, Ola; Nadon, Robert (April 1, 2009). "Gene Expression - Time to change point of view?". In Harding, Stephen (ed.). Biotechnology & Genetic Engineering Reviews. Vol. 25. Nottingham University Press. pp. 86–87. ISBN 9781904761662.
  30. ^ "Jack D. Keene, Ph.D." The Pew Charitable Trusts. Retrieved 23 February 2020.

August 31, 2023
jack, keene, born, june, 1947, jacksonville, florida, james, duke, professor, molecular, genetics, microbiology, duke, university, jack, donald, keenebornjack, donald, keene, 1947, june, 1947jacksonville, floridaalma, materuniversity, california, riverside, un. Jack D Keene born June 22 1947 Jacksonville Florida is a James B Duke Professor of Molecular Genetics and Microbiology at Duke University 1 Jack Donald KeeneBornJack Donald Keene 1947 06 22 June 22 1947Jacksonville FloridaAlma materUniversity of California Riverside University of WashingtonScientific careerInstitutionsDuke UniversityKeene studies the regulation of RNA and the mechanisms of RNA protein interactions 2 3 He identified RNA recognition motif RRM proteins which are the largest family of RNA binding proteins He isolated the first human autoimmune antigen He formalized the posttranscriptional operon and regulon PTRO model to describe global gene regulation and proposed the RNA regulon hypothesis to better understand post transcriptional regulation of mRNAs encoding proteins 3 4 Keene introduced the RIP ribonucleoprotein immunoprecipitation protocol for isolating specific mRNPs which has become a tool for the mapping of mRNA targets of specific RBPs 5 Contents 1 Early life and education 2 Career 3 Research 4 Awards and honors 5 ReferencesEarly life and education EditJack Donald Keene was born in Jacksonville Florida on June 22 1947 His father worked for the RAND Corporation 6 7 Keene attended Redlands High School in Redlands California graduating in 1965 1 Initially a student at University of California Los Angeles UCLA he transferred to the University of California Riverside where he majored in biology working with Carlton Bovell 6 He received his A B degree in 1969 7 Next Keene studied with Helen Riaboff Whiteley at the University of Washington in Seattle Washington graduating in 1975 with a doctorate in microbiology and Immunology 1 6 He did postdoctoral work in molecular virology with Robert A Lazzarini in the Laboratory for Molecular Genetics at the National Institutes of Health in Bethesda Maryland from 1974 to 1978 3 1 6 7 Career EditIn 1979 Keene was recruited by Wolfgang Joklik to the department of microbiology and immunology at Duke University Medical Center At that time the department was ranked one of the top three in the United States by the National Research Council 3 Keene was the chairman of the department of microbiology from 1992 to 2002 3 and director of basic sciences for the Duke Comprehensive Cancer Center from 1995 to 2003 7 As of 1997 he became the James B Duke Professor of Molecular Genetics and Microbiology at Duke University 8 In 1999 Keene founded the Duke Center for RNA Biology 1 Research EditKeene studies the regulation of RNA and the mechanisms of RNA protein interactions 2 9 10 In his work on molecular genetics he and his coworkers have examined the role of DNA and RNA binding proteins RBPs in the pathogenesis of autoimmunity 3 In the late 1970s and early 1980s he identified genomic sequences for vesicular stomatitis virus VSV and rabies virus RABV members of the Rhabdoviridae family of viruses 11 12 and for Ebola virus and Marburg virus from the broader group of negative strand RNA viruses NSRV 13 14 He identified the origins of defective interfering particles of negative strand RNA viruses 15 Through combinatorial studies of viral and bacterial systems he has identified targets for novel pharmacological studies 3 Later in the 1980s Keene identified RNA recognition motif RRM proteins RRM proteins are the largest family of RNA binding proteins and the seventh largest protein family of the human genome RRM is a prevalent RNA binding fold involving proteins implicated in RNA biogenesis processing transport and degradation 3 16 In 1987 Query and Keene first identified a B cell epitope within the U1 70K protein 17 18 Keene isolated the first human autoimmune antigen and elucidated its autoimmune epitopes the parts of an antigen to which antibodies in the immune system can bind 3 He cloned rheumatological autoimmune protein genes He developed a diagnostic test for systemic lupus erythematosus using recombinant antigens 3 19 20 Keene s lab has identified functions of the ELAV Hu posttranscriptional regulators HuB HuC and HuD and their roles and that of HuR in processes of growth proliferation differentiation and immune response 3 21 22 23 The study of RNA binding proteins such as HuR and the determination of the binding of specific sequences have informed Keene s later post transcription theory and his coordination theory of RNA operons 6 3 RNA binding proteins appear to be implicated in the functioning of many posttranscriptional processes As of 1994 Keene suggested that RNA binding proteins could be involved in the regulation of messenger RNA that encode cytokines In 2000 he was able to apply this approach to demonstrate neuronal differentiation 1 He also introduced the first use of the RIP ribonucleoprotein immunoprecipitation protocol isolating specific mRNPs using immunoprecipitation and identifying the mRNA component with microarray or deep sequencing This method has become a tool for the mapping of mRNA targets of specific RBPs 5 24 In 2001 2002 Keene formalized the posttranscriptional operon and regulon PTRO model for global gene regulation 3 25 26 By 2007 Keene proposed the RNA regulon hypothesis that mRNAs encoded by functionally related genes may be coordinately regulated as posttranscriptional RNA regulons by specific mRNP processing machineries 27 The purpose of the RNA regulon model was to better understand post transcriptional regulation to answer the question How does the cell coordinate metabolism and regulation of mRNAs encoding proteins in the same biological process so that the proteins can be coordinately produced 4 28 29 Awards and honors Edit1985 Pew Scholar in the Biomedical Sciences The Pew Charitable Trusts 30 2009 Fellow American Academy of Microbiology 6 2009 James Buchanan Duke Distinguished Professorship Duke University 6 2009 Member American Academy of Microbiology 6 References Edit a b c d e f Jack Keene PhD Biography Duke University Retrieved 5 November 2019 a b Doyle Francis Tenenbaum Scott A 15 April 2014 Trans regulation of RNA binding protein motifs by microRNA Frontiers in Genetics 5 79 doi 10 3389 fgene 2014 00079 PMC 4006066 PMID 24795744 a b c d e f g h i j k l m Hamilton John D February 10 2015 The History of Infectious Diseases At Duke University In the Twentieth Century Lulu Publishing Services pp 139 140 ISBN 9781483423753 Retrieved 23 February 2020 a b Culjkovic Kraljacic Biljana Borden Katherine L B 5 November 2018 The Impact of Post transcriptional Control Better Living Through RNA Regulons Frontiers in Genetics 9 512 doi 10 3389 fgene 2018 00512 PMC 6230556 PMID 30455716 a b Sanford Jeremy R Penalva Luiz O F 29 November 2017 The 3 end of the story deciphering combinatorial interactions that control mRNA fate Genome Biology 18 1 227 doi 10 1186 s13059 017 1360 6 PMC 5707901 PMID 29187223 a b c d e f g h Center for Oral History Jack D Keene Science History Institute a b c d Thackray Arnold Morris Stephanie Caruso David 2008 Jack D Keene Transcript of an Interview Conducted by Arnold Thackray Stephanie Morris and David Caruso at Ixtapa Mexico and Johns Hopkins University Baltimore Maryland on 5 March 1989 and 23 and 25 April 2008 Philadelphia PA Chemical Heritage Foundation Jack Donald Keene Scholars Duke University Retrieved 8 February 2020 Keene J D January 2007 Biological Clocks and the Coordination Theory of RNA Operons and Regulons Cold Spring Harbor Symposia on Quantitative Biology 72 1 157 165 doi 10 1101 sqb 2007 72 013 PMID 18419273 Keene Jack D April 2010 Minireview Global Regulation and Dynamics of Ribonucleic Acid Endocrinology 151 4 1391 1397 doi 10 1210 en 2009 1250 PMC 2850242 PMID 20332203 Wagner Robert R June 29 2013 The Rhabdoviruses Springer Science amp Business Media pp 139 140 ISBN 9781468470321 Keene J D Schubert M Lazzarini R A Rosenberg M 1 July 1978 Nucleotide sequence homology at the 3 termini of RNA from vesicular stomatitis virus and its defective interfering particles Proceedings of the National Academy of Sciences 75 7 3225 3229 Bibcode 1978PNAS 75 3225K doi 10 1073 pnas 75 7 3225 PMC 392747 PMID 210454 Deflube Laure R Cressey Tessa N Hume Adam J Olejnik Judith Haddock Elaine Feldmann Friederike Ebihara Hideki Fearns Rachel Muhlberger Elke 23 April 2019 Ebolavirus polymerase uses an unconventional genome replication mechanism Proceedings of the National Academy of Sciences 116 17 8535 8543 doi 10 1073 pnas 1815745116 PMC 6486738 PMID 30962389 Kiley Michael P Wilusz Jeffrey Mc Cormick Joseph B Keene Jack D March 1986 Conservation of the 3 terminal nucleotide sequences of Ebola and Marburg virus Virology 149 2 251 254 doi 10 1016 0042 6822 86 90127 3 PMID 3946083 Lazzarini Robert A Keene Jack D Schubert Manfred October 1981 The origins of defective interfering particles of the negative strand RNA viruses Cell 26 2 145 154 doi 10 1016 0092 8674 81 90298 1 PMID 7037195 Loerch Sarah Kielkopf Clara L September 2015 Dividing and Conquering the Family of RNA Recognition Motifs A Representative Case Based on hnRNP L Journal of Molecular Biology 427 19 2997 3000 doi 10 1016 j jmb 2015 06 009 PMC 4820351 PMID 26101840 Kattah Nicole H Kattah Michael G Utz Paul J January 2010 The U1 snRNP complex structural properties relating to autoimmune pathogenesis in rheumatic diseases Immunological Reviews 233 1 126 145 doi 10 1111 j 0105 2896 2009 00863 x PMC 3074261 PMID 20192997 Query C October 1987 A human autoimmune protein associated with U1 RNA contains a region of homology that is cross reactive with retroviral p30gag antigen Cell 51 2 211 220 doi 10 1016 0092 8674 87 90148 6 PMC 3074261 PMID 2959371 Habets WJ Hoet MH Sillekens PT De Rooij DJ Van de Putte LB Van Venrooij WJ May 1989 Detection of autoantibodies in a quantitative immunoassay using recombinant ribonucleoprotein antigens Clinical and Experimental Immunology 76 2 172 7 PMC 1541836 PMID 2527098 Chambers J C Keene J D 1 April 1985 Isolation and analysis of cDNA clones expressing human lupus La antigen Proceedings of the National Academy of Sciences 82 7 2115 2119 Bibcode 1985PNAS 82 2115C doi 10 1073 pnas 82 7 2115 PMC 397503 PMID 3856888 Simone Laura E Keene Jack D February 2013 Mechanisms coordinating ELAV Hu mRNA regulons Current Opinion in Genetics amp Development 23 1 35 43 doi 10 1016 j gde 2012 12 006 PMC 3617084 PMID 23312841 Bevilacqua Annamaria Ceriani Maria Cristina Capaccioli Sergio Nicolin Angelo June 2003 Post transcriptional regulation of gene expression by degradation of messenger RNAs Journal of Cellular Physiology 195 3 356 372 doi 10 1002 jcp 10272 PMID 12704645 Mansfield Kyle D Keene Jack D March 2012 Neuron specific ELAV Hu proteins suppress HuR mRNA during neuronal differentiation by alternative polyadenylation Nucleic Acids Research 40 6 2734 2746 doi 10 1093 nar gkr1114 PMC 3315332 PMID 22139917 Keene J D 19 June 2001 Ribonucleoprotein infrastructure regulating the flow of genetic information between the genome and the proteome Proceedings of the National Academy of Sciences 98 13 7018 7024 Bibcode 2001PNAS 98 7018K doi 10 1073 pnas 111145598 PMC 34616 PMID 11416181 Aparicio Luis A Abella Vanessa Valladares Manuel Figueroa Angelica 29 May 2013 Posttranscriptional regulation by RNA binding proteins during epithelial to mesenchymal transition Cellular and Molecular Life Sciences 70 23 4463 4477 doi 10 1007 s00018 013 1379 0 PMC 3827902 PMID 23715860 Keene Jack D July 2007 RNA regulons coordination of post transcriptional events PDF Nature Reviews Genetics 8 7 533 543 doi 10 1038 nrg2111 PMID 17572691 Retrieved 8 February 2020 Wang Li Miao Yi Liang Zheng Xiaofeng Lackford Brad Zhou Bingying Han Leng Yao Chengguo Ward James M Burkholder Adam Lipchina Inna Fargo David C Hochedlinger Konrad Shi Yongsheng Williams Carmen J Hu Guang December 2013 The THO Complex Regulates Pluripotency Gene mRNA Export and Controls Embryonic Stem Cell Self Renewal and Somatic Cell Reprogramming Cell Stem Cell 13 6 676 690 doi 10 1016 j stem 2013 10 008 PMC 3962795 PMID 24315442 Pulendran Bali Katsikis Peter D Schoenberger Stephen P eds August 19 2011 Crossroads between Innate and Adaptive Immunity III Springer Science amp Business Media pp 1 3 ISBN 9781441956323 Retrieved 24 February 2020 Larsson Ola Nadon Robert April 1 2009 Gene Expression Time to change point of view In Harding Stephen ed Biotechnology amp Genetic Engineering Reviews Vol 25 Nottingham University Press pp 86 87 ISBN 9781904761662 Jack D Keene Ph D The Pew Charitable Trusts Retrieved 23 February 2020 Retrieved from https en wikipedia org w index php title Jack D Keene amp oldid 1170978271, wikipedia, wiki, book, books, library,

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