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Repression of the RHOH gene by JunD
Abstract
RhoH is a member of the Rho family of small GTP-binding proteins that lacks GTPase activity. Since RhoH is constantly bound by GTP, it is thought to be constitutively active and controlled predominantly by changes in quantitative expression. RhoH is produced specifically in haematopoietic cells and aberrant expression has been linked to various forms of leukaemia. Transcription of the RHOH gene is the first level at which the quantitative levels of the RhoH protein are regulated. Previous studies have demonstrated that RHOH gene transcription is initiated by three distinct promoter regions designated P1, P2 and P3 that define the 5′ end of exons 1, 2 and 4 respectively. In the present study we report that the P3 promoter is largely responsible for RHOH gene transcription in the B-lymphocytic cell line Raji. The P3 promoter contains a minimal promoter region and a repressor region extending from −236 to +67 and +68 to +245 respectively, relative to the 5′ end of exon 4. Chromatin immunoprecipitation demonstrated that two AP1 (activator protein 1) sites in the minimal promoter region bind JunD. When JUND is overexpressed, the endogenous RHOH gene is repressed; however, when JUND is inhibited, expression of endogenous RHOH is induced both in the Raji cell line and AML (acute myeloid leukaemia) cells. In the HCL (hairy cell leukaemia) cell line JOK-1, induction of RHOH increases expression of the α isoform of protein kinase C. This downstream target of RHOH is also induced in AML cells by JUND inhibition. Collectively, these data indicate that JunD is an inhibitor of RHOH gene expression.
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In the citing paper
“RhoH remains in a constitutively active state and thus its effects are regulated by expression levels or post-translational modifications.”
From A Unique Carboxyl-terminal Insert Domain in the Hematopoietic-specific, GTPase-deficient Rho GTPase RhoH Regulates Post-translational Processing (2013) · cites this paper as [24]
In the citing paper
“Alternatively, its activation can be regulated by other types of regulation, including lysosomal degradation, somatic mutation and transcriptional repressor, which also results in an altered protein expression.”
From The Role of RhoH in TCR Signalling and Its Involvement in Diseases (2021) · cites this paper as [61]
In the citing paper
“However, because RhoH expression can be regulated by phosphorylation, lysosomal degradation and transcriptional repression by the AP−1 transcription factor, JunD [22,60,61], either of these regulations may be impaired in leukaemia.”
From The Role of RhoH in TCR Signalling and Its Involvement in Diseases (2021) · cites this paper as [61]
In the citing paper
“Consistent with this finding, overexpression of JunD was found to repress RhoH gene in AML [61,63], indicating that regulation of RhoH mRNA expression by a transcriptional repressor may affect RhoH anti-tumour activity.”
From The Role of RhoH in TCR Signalling and Its Involvement in Diseases (2021) · cites this paper as [61]
In the citing paper
“Consistent with this induction, expression of JunD that represses RHOH gene transcription is down‐regulated (Figure 4A, B) [14].”
From Bimodal expression of RHOH during myelomonocytic differentiation: Implications for the expansion of AML differentiation therapy (2021) · cites this paper as [14]
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Cites
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Involvement of RhoH GTPase in the development of B-cell chronic lymphocytic leukemia
Sanchez-Aguilera, A., Rattmann, I., Drew, D. Z., Müller, L. U. W., Summey, V, Lucas, D. M., Byrd, J. C., Croce, C. M., Gu, Y., Cancelas, J. A., et al. (2010) · Leukemia · doi:10.1038/leu.2009.217 · Cited by 52
Underexpression of RhoH in Hairy Cell Leukemia
Galiègue-Zouitina, S., Delestré, L., Dupont, C., Troussard, X., & Shelley, C. S. (2008) · Cancer Research · doi:10.1158/0008-5472.can-07-5661 · Cited by 34
Self-citationGündogdu, M. S., Liu, H., Metzdorf, D., Hildebrand, D., Aigner, M., Aktories, K., Heeg, K., & Kubatzky, K. F. (2010) · Molecular Cancer · doi:10.1186/1476-4598-9-225 · Cited by 29
RhoH Plays Critical Roles in FcεRI-Dependent Signal Transduction in Mast Cells
Oda, H., Fujimoto, M., Patrick, M. S., Chida, D., Sato, Y., Azuma, Y., Aoki, H., Abe, T., Suzuki, H., & Shirai, M. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.182.2.957 · Cited by 29
RhoH GTPase: A Key Regulator of Hematopoietic Cell Proliferation and Apoptosis?
Gu, Y., Zheng, Y., & Williams, D. A. (2005) · Cell Cycle · doi:10.4161/cc.4.2.1395 · Cited by 20
Lysosomal degradation of RhoH protein upon antigen receptor activation in T but not B cells
Schmidt‐Mende, J., Geering, B., Yousefi, S., & Simon, H. (2010) · European Journal of Immunology · doi:10.1002/eji.200939556 · Cited by 20
RhoH/TTF Negatively Regulates Leukotriene Production in Neutrophils
Daryadel, A., Yousefi, S., Troi, D., Schmid, I., Schmidt-Mende, J., Mordasini, C., Dahinden, C. A., Ziemiecki, A., & Simon, H.-U. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0803846 · Cited by 20
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Cited by
The Role of RhoH in TCR Signalling and Its Involvement in Diseases
Ahmad Mokhtar, A. M., Hashim, I. F., Mohd Zaini Makhtar, M., Salikin, N. H., & Amin-Nordin, S. (2021) · Cells · doi:10.3390/cells10040950 · Cited by 25
Troeger, A., Chae, H.-D., Senturk, M., Wood, J., & Williams, D. A. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.505727 · Cited by 15
Galiègue‐Zouitina, S., Fu, Q., Carton‐Latreche, C., Poret, N., Cheok, M., Leprêtre, F., Figeac, M., Quesnel, B., El Bouazzati, H., & Shelley, C. S. (2021) · eJHaem · doi:10.1002/jha2.128 · Cited by 7
Self-citation
Metadata
- Authors
- Delestré, L., Berthon, C., Quesnel, B., Figeac, M., Kerckaert, J.-P., Galiègue-Zouitina, S., & Shelley, C. S.
- Affiliations
- Institut National de la Santé et de la Recherche Médicale U.837, Centre Jean-Pierre Aubert, Institut pour la Recherche sur le Cancer de Lille and Université Lille Nord de France, UDSL, 59000 Lille, France
- Université Lille Nord de France, UDSL, Université de Lille 2, 59045 Lille, France
- Gundersen Lutheran Medical Foundation, La Crosse, WI 54601, U.S.A.
- Venue
- Biochemical Journal
- Publisher
- Portland Press Ltd.
- Published
- 2011-06-14
- Volume
- 437
- Issue
- 1
- Pages
- 75-88
- ISSN
- 0264-6021
- 1470-8728
- Cited by
- 13
- References
- 10
- Language
- en
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