scholarly journals Isolation and sequencing of the HMG domain of ten Sox genes from Odorrana schmackeri (Amphibia: Anura)

2009 ◽  
Vol 26 (1) ◽  
pp. 109-117
Author(s):  
Ning Wang ◽  
Jing J. Wang ◽  
Rui Jia ◽  
Jin W. Xu ◽  
Liu W. Nie
Keyword(s):  
2000 ◽  
Vol 28 (5) ◽  
pp. A186-A186
Author(s):  
K. Nagai

2020 ◽  
Author(s):  
Chia-Feng Liu ◽  
Ying Ng ◽  
Varun Thachil ◽  
Michael Morley ◽  
Christine S Moravec ◽  
...  

Abstract Background: The Sry-related high-mobility-group box (SOX) gene family, with 20 known transcription factors in humans, plays essential roles during development and in many disease processes. Several SOX proteins, e.g., SOX4, SOX11, and SOX9, are required for normal heart morphogenesis. SOX9 was shown to contribute to cardiac fibrosis in animal models. However, differential expression of other SOX transcription factors and their functional roles in the failing human myocardium have not been explored.Methods and Findings: All 20 SOX genes from RNA-seq data were extracted, and their RNA levels were compared to the NF, DCM, and hypertrophic cardiomyopathy (HCM) groups. The protein levels of the differential expressed SOX genes were confirmed by Western blot. Four SOX genes whose RNA levels were significantly upregulated in DCM or HCM compared to NF. However, only SOX4 and SOX8 proteins were markedly increased in the heart failure groups. Gene co-expression network analysis identified genes associated and respond similarly to perturbations with SOX4 in cardiac tissues. Using a meta-analysis combining epigenetics and genome-wide association data, we reported several genomic variants associated with HF phenotype linked to SOX4 or SOX8.Conclusions: Elevation of SOX8 and SOX4 are observed in the failing human myocardium. The molecular mechanism associated with them in HF warrants further investigation.


2006 ◽  
Vol 29 (3) ◽  
pp. 576-579 ◽  
Author(s):  
Li Jie ◽  
Ping-Ping Zheng ◽  
Jiao-Lian Song ◽  
Jin-Long Rui ◽  
Liu-Wang Nie
Keyword(s):  

2005 ◽  
Vol 15 (1) ◽  
pp. 7-13 ◽  
Author(s):  
Larysa Pevny ◽  
Marysia Placzek
Keyword(s):  

EvoDevo ◽  
2011 ◽  
Vol 2 (1) ◽  
pp. 12 ◽  
Author(s):  
Muriel Jager ◽  
Eric Quéinnec ◽  
Hervé Le Guyader ◽  
Michaël Manuel
Keyword(s):  

2008 ◽  
Vol 10 (5) ◽  
pp. 648-660 ◽  
Author(s):  
Judith M. de Bont ◽  
Johan M. Kros ◽  
Monique M.C.J. Passier ◽  
Roel E. Reddingius ◽  
Peter A.E. Sillevis Smitt ◽  
...  

2001 ◽  
Vol 109 (2) ◽  
pp. 371-375 ◽  
Author(s):  
Frédéric Crémazy ◽  
Philippe Berta ◽  
Franck Girard

Author(s):  
Luis Baudouin-Gonzalez ◽  
Anna Schoenauer ◽  
Amber Harper ◽  
Grace Blakeley ◽  
Michael Seiter ◽  
...  

AbstractThe Sox family of transcription factors regulate many different processes during metazoan development, including stem cell maintenance, nervous system specification and germline development. In addition, it has recently become apparent that SoxB genes are involved in embryonic segmentation in several arthropod species. Segmentation in arthropods occurs in two main ways: long germ animals form all segments at once, best exemplified in the well-studied Drosophila melanogaster system, and short germ animals form anterior segments simultaneously, with posterior segments added sequentially from a segment addition zone. In both D. melanogaster and the short germ beetle Tribolium castaneum, the SoxB gene Dichaete is required for correct segmentation and, more recently, we showed that a close relative of Dichaete, Sox21b-1, is required for the simultaneous formation of prosomal segments and sequential addition of opisthosomal segments in the spider Parasteatoda tepidariorum. Here we further analysed the function and expression of Sox21b-1 in P. tepidariorum. We found that while this gene regulates the generation of both prosomal and opisthosomal segments, it plays different roles in the formation of these tagma reflecting their contrasting modes of segmentation and deployment of gene regulatory networks with different architectures. To further investigate the evolution of Sox genes and their roles we characterised the repertoire of the gene family across several arachnid species with and without an ancestral whole genome duplication, and compared Sox expression between P. tepidariorum and the harvestman Phalangium opilio. The results suggest that Sox21b-1 was likely involved in segmentation ancestrally in arachnids, but that other Sox genes could also regulate this process in these animals. We also found that most Sox families have been retained as duplicates or ohnologs after WGD and evidence for potential subfunctionalisation and/or neofunctionalization events.


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