Margo Gebbie
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Margo Gebbie has a total of 19 co-authors. Here are the top co-authors by number of shared publications:
- Danielle A. Garsin
Department of Microbiology and Molecular Genetic, University of Texas Health Sciences Center at Houston, Houston USA
2 shared publications Jonathan R. Goodson
Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, Maryland, USA
2 shared publicationsMelissa R. Cruz
Department of Microbiology and Molecular Genetics, The University of Texas Health Science Center at Houston, Houston, Texas, USA
2 shared publications- Wade C. Winkler
Department of Chemistry and Biochemistry, University of Maryland, College Park , Maryland 20742
2 shared publications - Alexey Nesvizhskii
University of Michigan
1 shared publication - Ambro van Hoof
Department of Molecular Genetics and Center for RNA Biology, The Ohio State University, Columbus, USA
1 shared publication
Latest Publications
- 21 January 2021
- Published by Elsevier in Current Biology
- Vol. 31 (4) , 900-907.e6
Parthenolide Destabilizes Microtubules by Covalently Modifying Tubulin
- 21 January 2021
- Published by Elsevier in Current Biology
- Vol. 31 (4) , 900-907.e6
Parthenolide Destabilizes Microtubules by Covalently Modifying Tubulin
- 15 May 2019
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 201 (10) , e00703-18
Ethanolamine Utilization and Bacterial Microcompartment Formation Are Subject to Carbon Catabolite Repression
Ethanolamine (EA) is a compound commonly found in the gastrointestinal (GI) tract that can affect the behavior of human pathogens that can sense and utilize it, such as Enterococcus faecalis and Salmonella . Therefore, it is important to understand how the genes that govern EA utilization are regulated. In this work, we investigated two regulatory factors that control this process. One factor, a small RNA (sRNA), is shown to be important for generating the right levels of gene expression for maximum efficiency. The second factor, a transcriptional repressor, is important for preventing expression when other preferred sources of energy are available. Furthermore, a global bioinformatics analysis revealed that this second mechanism of transcriptional regulation likely operates on similar genes in related bacteria.
- 15 May 2019
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 201 (10) , e00703-18
Ethanolamine Utilization and Bacterial Microcompartment Formation Are Subject to Carbon Catabolite Repression
Ethanolamine (EA) is a compound commonly found in the gastrointestinal (GI) tract that can affect the behavior of human pathogens that can sense and utilize it, such as Enterococcus faecalis and Salmonella . Therefore, it is important to understand how the genes that govern EA utilization are regulated. In this work, we investigated two regulatory factors that control this process. One factor, a small RNA (sRNA), is shown to be important for generating the right levels of gene expression for maximum efficiency. The second factor, a transcriptional repressor, is important for preventing expression when other preferred sources of energy are available. Furthermore, a global bioinformatics analysis revealed that this second mechanism of transcriptional regulation likely operates on similar genes in related bacteria.
- 22 August 2014
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 345 (6199) , 937-940
A riboswitch-containing sRNA controls gene expression by sequestration of a response regulator
A dual-action RNA switch for expression: Riboswitches are short segments of RNA that bind small molecules and switch between two different conformations, thereby regulating gene expression (see the Perspective by Chen and Gottesman). DebRoy et al. and Mellin et al. find a new class of riboswitches—in two different species of bacteria—that are both part of and regulate the production of a noncoding RNA. Each riboswitch ensures that a particular metabolic pathway is only activated in the presence of an essential small-molecule cofactor. In the absence of the cofactor, the full-length non-coding RNA is made and binds a regulator protein, preventing the regulator protein from inappropriately activating the metabolic pathway. Science , this issue p. 937 and p. 940 ; see also p. 876
- 22 August 2014
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 345 (6199) , 937-940
A riboswitch-containing sRNA controls gene expression by sequestration of a response regulator
A dual-action RNA switch for expression: Riboswitches are short segments of RNA that bind small molecules and switch between two different conformations, thereby regulating gene expression (see the Perspective by Chen and Gottesman). DebRoy et al. and Mellin et al. find a new class of riboswitches—in two different species of bacteria—that are both part of and regulate the production of a noncoding RNA. Each riboswitch ensures that a particular metabolic pathway is only activated in the presence of an essential small-molecule cofactor. In the absence of the cofactor, the full-length non-coding RNA is made and binds a regulator protein, preventing the regulator protein from inappropriately activating the metabolic pathway. Science , this issue p. 937 and p. 940 ; see also p. 876
- 1 January 2014
- Published by Elsevier
- Vol. 549, 489-512
Assessing RNA Interactions with Proteins by DRaCALA
- 1 January 2014
- Published by Elsevier
- Vol. 549, 489-512
Assessing RNA Interactions with Proteins by DRaCALA