Assessment of the key regulatory genes and their interologs for Turner syndrome employing network approach
Open accessAbstract
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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Sex chromosome dosage sensitive genes on the X chromosome regulate specific networks of autosomal genes.
“There is also evidence that sex chromosome dosage sensitive genes on the X chromosome regulate specific networks of autosomal genes, indicating an organized regulatory gene network of genes on the X chromosome and autosomes.107,110”
From Clinical practice guidelines for the care of girls and women with Turner syndrome. (2024) · cites this paper as [110]
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References 65 · Cited by 30
- Authors
- Farooqui, A., Tazyeen, S., Ahmed, M. M., Alam, A., Ali, S., Malik, M. Z., Ali, S., & Ishrat, R.
- Affiliations
- Jamia Millia Islamia (IN)
- Corresponding author
- Ishrat, Romana
- ORCID
- Venue
- Scientific Reports
- Published
- 2018-07-04
- Volume
- 8
- Issue
- 1
- Pages
- 10091-10091
- ISSN
- 2045-2322 (ISSN-L)
- PMC
- PMC6031616
- OpenAlex
- W2809904006
- Cited by
- 30
- References
- 65
- Citations by year
- 2024: 4 · 2023: 6 · 2022: 7 · 2021: 6 · 2020: 2 · 2019: 4 · 2018: 1
- FWCI
- 1.16
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Scientific Reports (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, other-oa)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- Indian Council of Medical Research
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene Regulatory Network Analysis
- Keywords
- Turner syndrome, gene regulatory networks, interologs, KDM6A, brain-derived neurotrophic factor, WDR5, ASH2L, scale-free networks, hub genes, orthologs, protein-protein interaction
- MeSH terms
- Animals, DNA-Binding Proteins, Genes, Regulator, Humans, Nuclear Proteins, Histone-Lysine N-Methyltransferase, Transcription Factors, Turner Syndrome, Caenorhabditis elegans, Brain-Derived Neurotrophic Factor, Computational Biology, Intracellular Signaling Peptides and Proteins, Gene Regulatory Networks, Histone Demethylases, Protein Interaction Maps
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