PhotosBiographyFacebookTwitter

From Wikipedia, the free encyclopedia
Joachim Lingner
Joachim Lingner
Born1962 (age 61–62)
Nationality Swiss
Occupation Cell biology
Board member of
Awards
  • Friedrich Miescher Prize
  • ERC Advanced Investigator Award
Academic background
Alma mater University of Basel
Academic work
Discipline Cell biology
Institutions École Polytechnique Fédérale de Lausanne (EPFL)
Main interests
Website https://www.epfl.ch/labs/lingner-lab/

Joachim Lingner (born 1962) is a Swiss molecular biologist. He holds the professorship for life sciences and leads the Lingner Lab [1] at the École Polytechnique Fédérale de Lausanne (EPFL).

Career

Lingner obtained his PhD from the Biozentrum of the University of Basel in 1992. [2] In 1993 he joined the Howard Hughes Medical Institute at University of Colorado at Boulder for postdoctoral studies under the supervision of Thomas Cech. [3] He then joined Swiss Institute for Experimental Cancer Research (ISREC) in Lausanne, Switzerland, first as a junior group leader in 1997 and became senior group leader in 2002. In 2005 he was appointed as associate professor at EPF Lausanne. Since 2009, Lingner is a full professor at EPF Lausanne. [4] [5]

Research

The Lingner Lab studies of the structure, function and maintenance of telomeres, the nucleoprotein complexes at the ends of eukaryotic chromosomes that enable chromosome stability and that regulate cellular lifespan. They elucidated how telomere shortening is counteracted by the telomerase enzyme that renders cancer cells immortal. [6] [7] The lab discovered that telomeres are transcribed into telomeric repeat containing RNA (TERRA), [8] which in turn regulates the telomeric chromatin structure and telomere maintenance by telomerase and homology directed repair. [9] [10] Finally, they developed technologies to uncover the changes that occur in the telomeric proteome during aging and disease including cancer. [10] [11] [12]

Awards and recognitions

Lingner obtained the Friedrich Miescher Prize (2002), [13] was elected as an EMBO member (2005), [14] and received an ERC advanced investigator award (2008), [15] and is a member of the Academia Europaea (2020). [16]

He serves as a member of the scientific advisory board in the Center of Integrative Genomics (CIG) of the University of Lausanne, [17] and has been a member of ERC starting grant review panel. [18]

Selected works

References

  1. ^ "LINGNER LAB". www.epfl.ch. Retrieved 2020-09-02.
  2. ^ Lingner, Joachim; Kellermann, Josef; Keller, Walter (1991-12-12). "Cloning and expression of the essential gene for poly(A) polymerase from S. cerevisiae". Nature. 354 (6353): 496–498. Bibcode: 1991Natur.354..496L. doi: 10.1038/354496a0. ISSN  0028-0836. PMID  1840648. S2CID  2713293.
  3. ^ Lingner, J. (1997-04-25). "Reverse Transcriptase Motifs in the Catalytic Subunit of Telomerase". Science. 276 (5312): 561–567. doi: 10.1126/science.276.5312.561. PMID  9110970.
  4. ^ Teixeira, M.Teresa; Arneric, Milica; Sperisen, Peter; Lingner, Joachim (April 2004). "Telomere Length Homeostasis Is Achieved via a Switch between Telomerase- Extendible and -Nonextendible States". Cell. 117 (3): 323–335. doi: 10.1016/S0092-8674(04)00334-4. PMID  15109493. S2CID  18179591.
  5. ^ Chen, Liuh-Yow; Redon, Sophie; Lingner, Joachim (August 2012). "The human CST complex is a terminator of telomerase activity". Nature. 488 (7412): 540–544. Bibcode: 2012Natur.488..540C. doi: 10.1038/nature11269. ISSN  0028-0836. PMID  22763445. S2CID  4412583.
  6. ^ Teixeira, M.Teresa; Arneric, Milica; Sperisen, Peter; Lingner, Joachim (2004-04-30). "Telomere Length Homeostasis Is Achieved via a Switch between Telomerase- Extendible and -Nonextendible States". Cell. 117 (3): 323–335. doi: 10.1016/S0092-8674(04)00334-4. PMID  15109493. S2CID  18179591.
  7. ^ Chen, Liuh-Yow; Redon, Sophie; Lingner, Joachim (2012-07-04). "The human CST complex is a terminator of telomerase activity". Nature. 488 (7412): 540–544. Bibcode: 2012Natur.488..540C. doi: 10.1038/nature11269. ISSN  0028-0836. PMID  22763445. S2CID  4412583.
  8. ^ Azzalin, Claus M.; Lingner, Joachim (2007-08-30). "Damage control". Nature. 448 (7157): 1001–1002. doi: 10.1038/4481001a. ISSN  1476-4687. PMID  17728746. S2CID  37239103.
  9. ^ Porro, Antonio; Feuerhahn, Sascha; Lingner, Joachim (2014-02-27). "TERRA-Reinforced Association of LSD1 with MRE11 Promotes Processing of Uncapped Telomeres". Cell Reports. 6 (4): 765–776. doi: 10.1016/j.celrep.2014.01.022. PMID  24529708.
  10. ^ a b Vančevska, Aleksandra; Ahmed, Wareed; Pfeiffer, Verena; Feretzaki, Marianna; Boulton, Simon J; Lingner, Joachim (2020-04-01). "SMCHD1 promotes ATM-dependent DNA damage signaling and repair of uncapped telomeres". The EMBO Journal. 39 (7): e102668. doi: 10.15252/embj.2019102668. ISSN  0261-4189. PMC  7110143. PMID  32080884.
  11. ^ Grolimund, Larissa; Aeby, Eric; Hamelin, Romain; Armand, Florence; Chiappe, Diego; Moniatte, Marc; Lingner, Joachim (2013-11-25). "A quantitative telomeric chromatin isolation protocol identifies different telomeric states". Nature Communications. 4 (1): 2848. Bibcode: 2013NatCo...4.2848G. doi: 10.1038/ncomms3848. ISSN  2041-1723. PMID  24270157.
  12. ^ Ahmed, Wareed; Lingner, Joachim (2017-12-04). "Impact of oxidative stress on telomere biology". Differentiation. 99: 21–27. doi: 10.1016/j.diff.2017.12.002. PMID  29274896.
  13. ^ "Awards - Funding - LS²". www.ls2.ch. Retrieved 2020-09-02.
  14. ^ Katja. "Find a Member". EMBO. Retrieved 2020-09-02.[ permanent dead link]
  15. ^ https://erc.europa.eu/sites/default/files/content/selection_panel/advanced_grant_2008.pdf [ bare URL PDF]
  16. ^ "List all members by country".
  17. ^ "Scientific Advisory Committee". www.unil.ch. Retrieved 2020-09-02.
  18. ^ https://erc.europa.eu/sites/default/files/document/file/erc_2018_stg_panel_members.pdf [ bare URL PDF]
From Wikipedia, the free encyclopedia
Joachim Lingner
Joachim Lingner
Born1962 (age 61–62)
Nationality Swiss
Occupation Cell biology
Board member of
Awards
  • Friedrich Miescher Prize
  • ERC Advanced Investigator Award
Academic background
Alma mater University of Basel
Academic work
Discipline Cell biology
Institutions École Polytechnique Fédérale de Lausanne (EPFL)
Main interests
Website https://www.epfl.ch/labs/lingner-lab/

Joachim Lingner (born 1962) is a Swiss molecular biologist. He holds the professorship for life sciences and leads the Lingner Lab [1] at the École Polytechnique Fédérale de Lausanne (EPFL).

Career

Lingner obtained his PhD from the Biozentrum of the University of Basel in 1992. [2] In 1993 he joined the Howard Hughes Medical Institute at University of Colorado at Boulder for postdoctoral studies under the supervision of Thomas Cech. [3] He then joined Swiss Institute for Experimental Cancer Research (ISREC) in Lausanne, Switzerland, first as a junior group leader in 1997 and became senior group leader in 2002. In 2005 he was appointed as associate professor at EPF Lausanne. Since 2009, Lingner is a full professor at EPF Lausanne. [4] [5]

Research

The Lingner Lab studies of the structure, function and maintenance of telomeres, the nucleoprotein complexes at the ends of eukaryotic chromosomes that enable chromosome stability and that regulate cellular lifespan. They elucidated how telomere shortening is counteracted by the telomerase enzyme that renders cancer cells immortal. [6] [7] The lab discovered that telomeres are transcribed into telomeric repeat containing RNA (TERRA), [8] which in turn regulates the telomeric chromatin structure and telomere maintenance by telomerase and homology directed repair. [9] [10] Finally, they developed technologies to uncover the changes that occur in the telomeric proteome during aging and disease including cancer. [10] [11] [12]

Awards and recognitions

Lingner obtained the Friedrich Miescher Prize (2002), [13] was elected as an EMBO member (2005), [14] and received an ERC advanced investigator award (2008), [15] and is a member of the Academia Europaea (2020). [16]

He serves as a member of the scientific advisory board in the Center of Integrative Genomics (CIG) of the University of Lausanne, [17] and has been a member of ERC starting grant review panel. [18]

Selected works

References

  1. ^ "LINGNER LAB". www.epfl.ch. Retrieved 2020-09-02.
  2. ^ Lingner, Joachim; Kellermann, Josef; Keller, Walter (1991-12-12). "Cloning and expression of the essential gene for poly(A) polymerase from S. cerevisiae". Nature. 354 (6353): 496–498. Bibcode: 1991Natur.354..496L. doi: 10.1038/354496a0. ISSN  0028-0836. PMID  1840648. S2CID  2713293.
  3. ^ Lingner, J. (1997-04-25). "Reverse Transcriptase Motifs in the Catalytic Subunit of Telomerase". Science. 276 (5312): 561–567. doi: 10.1126/science.276.5312.561. PMID  9110970.
  4. ^ Teixeira, M.Teresa; Arneric, Milica; Sperisen, Peter; Lingner, Joachim (April 2004). "Telomere Length Homeostasis Is Achieved via a Switch between Telomerase- Extendible and -Nonextendible States". Cell. 117 (3): 323–335. doi: 10.1016/S0092-8674(04)00334-4. PMID  15109493. S2CID  18179591.
  5. ^ Chen, Liuh-Yow; Redon, Sophie; Lingner, Joachim (August 2012). "The human CST complex is a terminator of telomerase activity". Nature. 488 (7412): 540–544. Bibcode: 2012Natur.488..540C. doi: 10.1038/nature11269. ISSN  0028-0836. PMID  22763445. S2CID  4412583.
  6. ^ Teixeira, M.Teresa; Arneric, Milica; Sperisen, Peter; Lingner, Joachim (2004-04-30). "Telomere Length Homeostasis Is Achieved via a Switch between Telomerase- Extendible and -Nonextendible States". Cell. 117 (3): 323–335. doi: 10.1016/S0092-8674(04)00334-4. PMID  15109493. S2CID  18179591.
  7. ^ Chen, Liuh-Yow; Redon, Sophie; Lingner, Joachim (2012-07-04). "The human CST complex is a terminator of telomerase activity". Nature. 488 (7412): 540–544. Bibcode: 2012Natur.488..540C. doi: 10.1038/nature11269. ISSN  0028-0836. PMID  22763445. S2CID  4412583.
  8. ^ Azzalin, Claus M.; Lingner, Joachim (2007-08-30). "Damage control". Nature. 448 (7157): 1001–1002. doi: 10.1038/4481001a. ISSN  1476-4687. PMID  17728746. S2CID  37239103.
  9. ^ Porro, Antonio; Feuerhahn, Sascha; Lingner, Joachim (2014-02-27). "TERRA-Reinforced Association of LSD1 with MRE11 Promotes Processing of Uncapped Telomeres". Cell Reports. 6 (4): 765–776. doi: 10.1016/j.celrep.2014.01.022. PMID  24529708.
  10. ^ a b Vančevska, Aleksandra; Ahmed, Wareed; Pfeiffer, Verena; Feretzaki, Marianna; Boulton, Simon J; Lingner, Joachim (2020-04-01). "SMCHD1 promotes ATM-dependent DNA damage signaling and repair of uncapped telomeres". The EMBO Journal. 39 (7): e102668. doi: 10.15252/embj.2019102668. ISSN  0261-4189. PMC  7110143. PMID  32080884.
  11. ^ Grolimund, Larissa; Aeby, Eric; Hamelin, Romain; Armand, Florence; Chiappe, Diego; Moniatte, Marc; Lingner, Joachim (2013-11-25). "A quantitative telomeric chromatin isolation protocol identifies different telomeric states". Nature Communications. 4 (1): 2848. Bibcode: 2013NatCo...4.2848G. doi: 10.1038/ncomms3848. ISSN  2041-1723. PMID  24270157.
  12. ^ Ahmed, Wareed; Lingner, Joachim (2017-12-04). "Impact of oxidative stress on telomere biology". Differentiation. 99: 21–27. doi: 10.1016/j.diff.2017.12.002. PMID  29274896.
  13. ^ "Awards - Funding - LS²". www.ls2.ch. Retrieved 2020-09-02.
  14. ^ Katja. "Find a Member". EMBO. Retrieved 2020-09-02.[ permanent dead link]
  15. ^ https://erc.europa.eu/sites/default/files/content/selection_panel/advanced_grant_2008.pdf [ bare URL PDF]
  16. ^ "List all members by country".
  17. ^ "Scientific Advisory Committee". www.unil.ch. Retrieved 2020-09-02.
  18. ^ https://erc.europa.eu/sites/default/files/document/file/erc_2018_stg_panel_members.pdf [ bare URL PDF]

Videos

Youtube | Vimeo | Bing

Websites

Google | Yahoo | Bing

Encyclopedia

Google | Yahoo | Bing

Facebook