Literature DB >> 20472563

Anti-steroidogenic factor ARR19 inhibits testicular steroidogenesis through the suppression of Nur77 transactivation.

Imteyaz Qamar1, Eun-Yeung Gong, Yeawon Kim, Chin-Hee Song, Hyun Joo Lee, Sang-Young Chun, Keesook Lee.   

Abstract

ARR19 (androgen receptor corepressor-19 kDa), a leucine-rich protein whose expression is down-regulated by luteinizing hormone and cAMP, is differentially expressed during the development of Leydig cells and inhibits testicular steroidogenesis by reducing the expression of steroidogenic enzymes. However, the molecular events behind the suppression of testicular steroidogenesis are unknown. In the present study, we demonstrate that ARR19 inhibits the transactivation of orphan nuclear receptor Nur77, which is one of the major transcription factors that regulate the expression of steroidogenic enzyme genes in Leydig cells. ARR19 physically interacts with Nur77 and suppresses Nur77-induced promoter activity of steroidogenic enzyme genes including StAR, P450c17, and 3beta-HSD in Leydig cells. Transient transfection and chromatin immunoprecipitation assays revealed that ARR19-mediated reduced expression of steroidogenic enzyme genes was likely due to the interference of SRC-1 recruitment to Nur77 protein on the promoter of steroidogenic enzyme genes. These findings suggest that ARR19 acts as a novel coregulator of Nur77, in turn regulating Nur77-induced testicular steroidogenesis, and may play an important role in the development and function of testicular Leydig cells.

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Year:  2010        PMID: 20472563      PMCID: PMC2903400          DOI: 10.1074/jbc.M109.059949

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  45 in total

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Journal:  Methods       Date:  2002-01       Impact factor: 3.608

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Authors:  K H Song; J I Park; M O Lee; J Soh; K Lee; H S Choi
Journal:  Endocrinology       Date:  2001-12       Impact factor: 4.736

5.  Gonadotropin regulation of NGFI-B messenger ribonucleic acid expression during ovarian follicle development in the rat.

Authors:  J I Park; H J Park; H S Choi; K Lee; W K Lee; S Y Chun
Journal:  Endocrinology       Date:  2001-07       Impact factor: 4.736

6.  Arachidonic acid release from rat Leydig cells depends on the presence of luteinizing hormone/human chorionic gonadotrophin receptors.

Authors:  P F Moraga; M N Llanos; A M Ronco
Journal:  J Endocrinol       Date:  1997-08       Impact factor: 4.286

7.  Silencing mediator of retinoid and thyroid hormone receptors and activating signal cointegrator-2 as transcriptional coregulators of the orphan nuclear receptor Nur77.

Authors:  Y C Sohn; E Kwak; Y Na; J W Lee; S K Lee
Journal:  J Biol Chem       Date:  2001-09-14       Impact factor: 5.157

Review 8.  Differentiation of the adult Leydig cell population in the postnatal testis.

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Journal:  Biol Reprod       Date:  2001-09       Impact factor: 4.285

Review 9.  Function of steroidogenic factor 1 during development and differentiation of the reproductive system.

Authors:  Y Sadovsky; C Dorn
Journal:  Rev Reprod       Date:  2000-09

Review 10.  The lutropin/choriogonadotropin receptor, a 2002 perspective.

Authors:  Mario Ascoli; Francesca Fanelli; Deborah L Segaloff
Journal:  Endocr Rev       Date:  2002-04       Impact factor: 19.871

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  9 in total

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Journal:  Biol Trace Elem Res       Date:  2022-10-10       Impact factor: 4.081

4.  Transforming growth factor-β1 signaling represses testicular steroidogenesis through cross-talk with orphan nuclear receptor Nur77.

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5.  Testis-Specific GTPase (TSG): An oligomeric protein.

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Journal:  BMC Genomics       Date:  2016-10-10       Impact factor: 3.969

6.  Nandrolone decanoate interferes with testosterone biosynthesis altering blood-testis barrier components.

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7.  Jagged1 intracellular domain modulates steroidogenesis in testicular Leydig cells.

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Journal:  PLoS One       Date:  2020-12-30       Impact factor: 3.240

8.  Divergence of mammalian higher order chromatin structure is associated with developmental loci.

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9.  A time-course study of long term over-expression of ARR19 in mice.

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