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Assessment of the key regulatory genes and their Interologs for Turner Syndrome employing network approach

Turner Syndrome (TS) is a condition where several genes are affected but the molecular mechanism remains unknown. Identifying the genes that regulate the TS network is one of the main challenges in understanding its aetiology. Here, we studied the regulatory network from manually curated genes repor...

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Autores principales: Farooqui, Anam, Tazyeen, Safia, Ahmed, Mohd. Murshad, Alam, Aftab, Ali, Shahnawaz, Malik, Md. Zubbair, Ali, Sher, Ishrat, Romana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031616/
https://www.ncbi.nlm.nih.gov/pubmed/29973620
http://dx.doi.org/10.1038/s41598-018-28375-0
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author Farooqui, Anam
Tazyeen, Safia
Ahmed, Mohd. Murshad
Alam, Aftab
Ali, Shahnawaz
Malik, Md. Zubbair
Ali, Sher
Ishrat, Romana
author_facet Farooqui, Anam
Tazyeen, Safia
Ahmed, Mohd. Murshad
Alam, Aftab
Ali, Shahnawaz
Malik, Md. Zubbair
Ali, Sher
Ishrat, Romana
author_sort Farooqui, Anam
collection PubMed
description Turner Syndrome (TS) is a condition where several genes are affected but the molecular mechanism remains unknown. Identifying the genes that regulate the TS network is one of the main challenges in understanding its aetiology. Here, we studied the regulatory network from manually curated genes reported in the literature and identified essential proteins involved in TS. The power-law distribution analysis showed that TS network carries scale-free hierarchical fractal attributes. This organization of the network maintained the self-ruled constitution of nodes at various levels without having centrality–lethality control systems. Out of twenty-seven genes culminating into leading hubs in the network, we identified two key regulators (KRs) i.e. KDM6A and BDNF. These KRs serve as the backbone for all the network activities. Removal of KRs does not cause its breakdown, rather a change in the topological properties was observed. Since essential proteins are evolutionarily conserved, the orthologs of selected interacting proteins in C. elegans, cat and macaque monkey (lower to higher level organisms) were identified. We deciphered three important interologs i.e. KDM6A-WDR5, KDM6A-ASH2L and WDR5-ASH2L that form a triangular motif. In conclusion, these KRs and identified interologs are expected to regulate the TS network signifying their biological importance.
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spelling pubmed-60316162018-07-12 Assessment of the key regulatory genes and their Interologs for Turner Syndrome employing network approach Farooqui, Anam Tazyeen, Safia Ahmed, Mohd. Murshad Alam, Aftab Ali, Shahnawaz Malik, Md. Zubbair Ali, Sher Ishrat, Romana Sci Rep Article Turner Syndrome (TS) is a condition where several genes are affected but the molecular mechanism remains unknown. Identifying the genes that regulate the TS network is one of the main challenges in understanding its aetiology. Here, we studied the regulatory network from manually curated genes reported in the literature and identified essential proteins involved in TS. The power-law distribution analysis showed that TS network carries scale-free hierarchical fractal attributes. This organization of the network maintained the self-ruled constitution of nodes at various levels without having centrality–lethality control systems. Out of twenty-seven genes culminating into leading hubs in the network, we identified two key regulators (KRs) i.e. KDM6A and BDNF. These KRs serve as the backbone for all the network activities. Removal of KRs does not cause its breakdown, rather a change in the topological properties was observed. Since essential proteins are evolutionarily conserved, the orthologs of selected interacting proteins in C. elegans, cat and macaque monkey (lower to higher level organisms) were identified. We deciphered three important interologs i.e. KDM6A-WDR5, KDM6A-ASH2L and WDR5-ASH2L that form a triangular motif. In conclusion, these KRs and identified interologs are expected to regulate the TS network signifying their biological importance. Nature Publishing Group UK 2018-07-04 /pmc/articles/PMC6031616/ /pubmed/29973620 http://dx.doi.org/10.1038/s41598-018-28375-0 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Farooqui, Anam
Tazyeen, Safia
Ahmed, Mohd. Murshad
Alam, Aftab
Ali, Shahnawaz
Malik, Md. Zubbair
Ali, Sher
Ishrat, Romana
Assessment of the key regulatory genes and their Interologs for Turner Syndrome employing network approach
title Assessment of the key regulatory genes and their Interologs for Turner Syndrome employing network approach
title_full Assessment of the key regulatory genes and their Interologs for Turner Syndrome employing network approach
title_fullStr Assessment of the key regulatory genes and their Interologs for Turner Syndrome employing network approach
title_full_unstemmed Assessment of the key regulatory genes and their Interologs for Turner Syndrome employing network approach
title_short Assessment of the key regulatory genes and their Interologs for Turner Syndrome employing network approach
title_sort assessment of the key regulatory genes and their interologs for turner syndrome employing network approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031616/
https://www.ncbi.nlm.nih.gov/pubmed/29973620
http://dx.doi.org/10.1038/s41598-018-28375-0
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