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Makale detayı · 2018 · article

Glioma tumor suppressor candidate region gene 1 (GLTSCR1) and its paralog GLTSCR1-like form SWI/SNF chromatin remodeling subcomplexes

ISSN0021-9258
YÖKSİS OpenAlex Açık erişim · hybrid Üst %10
Yıl2018
Atıf238OpenAlex
Atıf192Semantic Scholar · 8 etkili
Yüzdelik%98,2
FWCI7,361,00 = dünya ortalaması
Scopus (SJR)Q1
WoS (JCR)Q2

Veri kaynağı ayrımı

  • YÖKSİSYÖKSİS makale kaydı
  • YÖKSİS dergi adıJOURNAL OF BIOLOGICAL CHEMISTRY
  • Katalog eşleşmesi (ISSN)Journal of Biological Chemistry
  • OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)
  • Semantic Scholaratıf sayısı (OpenAlex ile birleştirilmez)

Özet

OpenAlex İngilizce

The mammalian SWI/SNF chromatin remodeling complex is a heterogeneous collection of related protein complexes required for gene regulation and genome integrity. It contains a central ATPase (BRM or BRG1) and various combinations of 10–14 accessory subunits (BAFs for BRM/BRG1 Associated Factors). Two distinct complexes differing in size, BAF and the slightly larger polybromo-BAF (PBAF), share many of the same core subunits but are differentiated primarily by having either AT-rich interaction domain 1A/B (ARID1A/B in BAF) or ARID2 (in PBAF). Using density gradient centrifugation and immunoprecipitation, we have identified and characterized a third and smaller SWI/SNF subcomplex. We termed this complex GBAF because it incorporates two mutually exclusive paralogs, GLTSCR1 (glioma tumor suppressor candidate region gene 1) or GLTSCR1L (GLTSCR1-like), instead of an ARID protein. In addition to GLTSCR1 or GLTSCR1L, the GBAF complex contains BRD9 (bromodomain-containing 9) and the BAF subunits BAF155, BAF60, SS18, BAF53a, and BRG1/BRM. We observed that GBAF does not contain the core BAF subunits BAF45, BAF47, or BAF57. Even without these subunits, GBAF displayed in vitro ATPase activity and bulk chromatin affinity comparable to those of BAF. GBAF associated with BRD4, but, unlike BRD4, the GBAF component GLTSCR1 was not required for the viability of the LNCaP prostate cancer cell line. In contrast, GLTSCR1 or GLTSCR1L knockouts in the metastatic prostate cancer cell line PC3 resulted in a loss in proliferation and colony-forming ability. Taken together, our results provide evidence for a compositionally novel SWI/SNF subcomplex with cell type–specific functions.

Konular

Atıflar

OpenAlex cited_by_count. WoS veya Scopus atıf sayısı değildir; o kaynaklar için ayrı kolon yoktur.

238atıfOpenAlex · cited_by_count (önbellek / veritabanı)

Yerel katalogda bu makaleye atıf yapan 7 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

  1. 2021 BRD9 Is a Critical Regulator of Androgen Receptor Signaling and Prostate Cancer ProgressionAtıf 75 · OpenAlex
  2. 2022 Altered BAF occupancy and transcription factor dynamics in PBAF-deficient melanomaAtıf 43 · OpenAlex
  3. 2022 BRD9-containing non-canonical BAF complex maintains somatic cell transcriptome and acts as a barrier to human reprogrammingAtıf 24 · OpenAlex
  4. 2024 Identification of SWI/SNF Subcomplex GBAF Presence, Intra-Complex Interactions, and Transcriptional Dynamics during Early Porcine DevelopmentAtıf 1 · OpenAlex
  5. 2024 Identification of SWI/SNF Subcomplex GBAF Presence, Intra-Complex Interactions, and Transcriptional Dynamics during Early Porcine DevelopmentAtıf 1 · OpenAlex
  6. 2021 BRD9-containing non-canonical BAF complexes safeguard cell identity and prevent reprogrammingAtıf 1 · OpenAlex
  7. 2023 Data from BRD9 Is a Critical Regulator of Androgen Receptor Signaling and Prostate Cancer ProgressionAtıf 0 · OpenAlex

Yazarlar

2
  1. AKTAN ALPSOY ORTA DOĞU TEKNİK ÜNİVERSİTESİ 1
  2. Emily C. Dykhuizen 2