CellStructureMech

LYSP100-associated nuclear domain

GO:0016606 · Other · Other · Proposed

A nuclear body that is enriched in the lymphoid cell-specific protein LYSp100B; LANDs are globular, electron-dense structures and are morphologically distinct from the annular structures characteristic of PML bodies. [GO:0016606]

Synonyms: LANDs

Part of: nuclear lumen (GO:0031981)

UniProt location names: UniProt Consortium, CC BY 4.0. Reference label and route sources.

Components

ComponentTypePart of / acts onGroundingGenesStoichiometryEssentialRole
LYSp100B/Sp140Proteinpart ofReviewed label only (reviewed name; no accession asserted)SP140UNKNOWNLymphoid-cell SP100 homolog that concentrates in LANDs and can be redistributed by the Bright/ARID3A transcription factor.
  • PMID:8695863 Dent et al. 1996 cloned human LYSP100 and localized LYSP100 protein to LAND nuclear dots that were mostly nonoverlapping with PML nuclear bodies.
  • DOI:10.1093/emboj/19.15.4123 Zong, Das and Tucker 2000 analyzed the LYSp100B/Sp140 homolog of Sp100 and its redistribution from LANDs after interaction with Bright.

Taxonomic distribution

Canonical examples

Functions

Mechanism graphs

LYSp100B marks LANDs and is redistributed by Bright (REGULATION)

LYSp100B/Sp140 concentrates in globular LAND nuclear domains distinct from PML bodies and can redistribute from LANDs when it interacts with the Bright/ARID3A immunoglobulin transcription factor.

SubjectPredicateObjectEvidence
LYSp100B/Sp140localizes toLYSP100-associated nuclear domain
  • PMID:8695863 Dent et al. 1996 used immunofluorescence and immunoelectron microscopy to localize LYSP100 to LANDs.
LYSP100-associated nuclear domainis distinct fromPML body
  • GO:0016606 GO:0016606 defines LANDs as morphologically distinct from PML bodies.
  • PMID:8695863 Dent et al. 1996 described the morphological and biochemical distinction between LANDs and PML bodies.
Bright/ARID3AredistributesLYSp100B/Sp140
LYSp100B/Sp140modulatesIgH enhancer transactivation
  • DOI:10.1093/emboj/19.15.4123 Zong, Das and Tucker 2000 found that LYSp100B strongly stimulated Bright transactivation through the E mu enhancer.

Discussions

Evidence

Curation history

Source: data/structures/other/lysp100_associated_nuclear_domain.yaml