HMGN1

Last updated
HMGN1
Identifiers
Aliases HMGN1 , HMG14, high mobility group nucleosome binding domain 1
External IDs OMIM: 163920 MGI: 96120 HomoloGene: 3643 GeneCards: HMGN1
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004965

NM_008251

RefSeq (protein)

NP_004956

NP_032277

Location (UCSC) Chr 21: 39.34 – 39.35 Mb Chr 16: 95.92 – 95.93 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Non-histone chromosomal protein HMG-14 is a protein that in humans is encoded by the HMGN1 gene. [5] [6] [7]

Contents

Function

Chromosomal protein HMG14 and its close analog HMG17 (MIM 163910) bind to the inner side of the nucleosomal DNA, potentially altering the interaction between the DNA and the histone octamer. The 2 proteins may be involved in the process that maintains transcribable genes in a unique chromatin conformation. [8] Their ubiquitous distribution and relative abundance, as well as the high evolutionary conservation of the DNA-binding domain of the HMG14 family of proteins, suggest that they may be involved in an important cellular function. [7]

Interactions

HMGN1 has been shown to interact with YWHAZ. [9]

See also

Related Research Articles

Chromatin is a complex of DNA and protein found in eukaryotic cells. The primary function is to package long DNA molecules into more compact, denser structures. This prevents the strands from becoming tangled and also plays important roles in reinforcing the DNA during cell division, preventing DNA damage, and regulating gene expression and DNA replication. During mitosis and meiosis, chromatin facilitates proper segregation of the chromosomes in anaphase; the characteristic shapes of chromosomes visible during this stage are the result of DNA being coiled into highly condensed chromatin.

HMGN proteins are members of the broader class of high mobility group (HMG) chromosomal proteins that are involved in regulation of transcription, replication, recombination, and DNA repair.

<span class="mw-page-title-main">Histone H1</span> Components of chromatin in eukaryotic cells

Histone H1 is one of the five main histone protein families which are components of chromatin in eukaryotic cells. Though highly conserved, it is nevertheless the most variable histone in sequence across species.

Chromatin remodeling is the dynamic modification of chromatin architecture to allow access of condensed genomic DNA to the regulatory transcription machinery proteins, and thereby control gene expression. Such remodeling is principally carried out by 1) covalent histone modifications by specific enzymes, e.g., histone acetyltransferases (HATs), deacetylases, methyltransferases, and kinases, and 2) ATP-dependent chromatin remodeling complexes which either move, eject or restructure nucleosomes. Besides actively regulating gene expression, dynamic remodeling of chromatin imparts an epigenetic regulatory role in several key biological processes, egg cells DNA replication and repair; apoptosis; chromosome segregation as well as development and pluripotency. Aberrations in chromatin remodeling proteins are found to be associated with human diseases, including cancer. Targeting chromatin remodeling pathways is currently evolving as a major therapeutic strategy in the treatment of several cancers.

<span class="mw-page-title-main">HMGA1</span> Protein-coding gene in the species Homo sapiens

High-mobility group protein HMG-I/HMG-Y is a protein that in humans is encoded by the HMGA1 gene.

<span class="mw-page-title-main">H3F3A</span> Gene for histone H3.3 protein

Histone H3.3 is a protein that in humans is encoded by the H3F3A and H3F3B genes. It plays an essential role in maintaining genome integrity during mammalian development.

<span class="mw-page-title-main">HIST1H3B</span> Protein-coding gene in the species Homo sapiens

Histone H3.1 is a protein that in humans is encoded by the H3C2 gene.

<span class="mw-page-title-main">Structure specific recognition protein 1</span> Protein-coding gene in the species Homo sapiens

FACT complex subunit SSRP1 also known as structure specific recognition protein 1 is a protein that in humans is encoded by the SSRP1 gene.

<span class="mw-page-title-main">HMGB2</span> Protein-coding gene in the species Homo sapiens

High-mobility group protein B2 also known as high-mobility group protein 2 (HMG-2) is a protein that in humans is encoded by the HMGB2 gene.

<span class="mw-page-title-main">H2AFY</span> Protein-coding gene in the species Homo sapiens

Core histone macro-H2A.1 is a protein that in humans is encoded by the H2AFY gene.

<span class="mw-page-title-main">HIST3H2BB</span> Protein-coding gene in the species Homo sapiens

Histone H2B type 3-B is a protein that in humans is encoded by the HIST3H2BB gene.

<span class="mw-page-title-main">HMGN2</span> Protein-coding gene in the species Homo sapiens

Non-histone chromosomal protein HMG-17 is a protein that in humans is encoded by the HMGN2 gene.

<span class="mw-page-title-main">RPS6KA4</span> Enzyme found in humans

Ribosomal protein S6 kinase alpha-4 is an enzyme that in humans is encoded by the RPS6KA4 gene.

<span class="mw-page-title-main">HMGN3</span> Protein-coding gene in the species Homo sapiens

High mobility group nucleosome-binding domain-containing protein 3 is a protein that in humans is encoded by the HMGN3 gene.

High mobility group protein HMG14 and HMG17 also known as nucleosomal binding domain is a family of evolutionarily related proteins.

<span class="mw-page-title-main">HMGN4</span> Protein-coding gene in the species Homo sapiens

High mobility group nucleosome-binding domain-containing protein 4 is a transcription factor that in humans is encoded by the HMGN4 gene.

<span class="mw-page-title-main">FOXA2</span> Mammalian protein found in Homo sapiens

Forkhead box protein A2 (FOXA2), also known as hepatocyte nuclear factor 3-beta (HNF-3B), is a transcription factor that plays an important role during development, in mature tissues and, when dysregulated or mutated, also in cancer.

<span class="mw-page-title-main">H2AFB3</span> Protein-coding gene in the species Homo sapiens

H2A histone family, member B3 is a protein that in humans is encoded by the H2AFB3 gene.

<span class="mw-page-title-main">H2BFWT</span> Protein-coding gene in the species Homo sapiens

H2B histone family, member W, testis-specific is a protein that in humans is encoded by the H2BFWT gene.

<span class="mw-page-title-main">HIST1H4J</span> Protein-coding gene in the species Homo sapiens

Histone cluster 1, H4j is a protein that in humans is encoded by the HIST1H4J gene.

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000205581 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000040681 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Landsman D, Srikantha T, Westermann R, Bustin M (Dec 1986). "Chromosomal protein HMG-14. Complete human cDNA sequence and evidence for a multigene family". The Journal of Biological Chemistry. 261 (34): 16082–6. doi: 10.1016/S0021-9258(18)66680-3 . PMID   3782107.
  6. Landsman D, McBride OW, Soares N, Crippa MP, Srikantha T, Bustin M (Feb 1989). "Chromosomal protein HMG-14. Identification, characterization, and chromosome localization of a functional gene from the large human multigene family". The Journal of Biological Chemistry. 264 (6): 3421–7. doi: 10.1016/S0021-9258(18)94084-6 . PMID   2563381.
  7. 1 2 "Entrez Gene: HMGN1 high-mobility group nucleosome binding domain 1".
  8. Martínez de Paz A, Ausió J (2016). "HMGNs: The enhancer charmers". BioEssays. 38 (3): 226–31. doi: 10.1002/bies.201500157 . PMID   26709929. S2CID   24768724.
  9. Prymakowska-Bosak M, Hock R, Catez F, Lim JH, Birger Y, Shirakawa H, Lee K, Bustin M (Oct 2002). "Mitotic phosphorylation of chromosomal protein HMGN1 inhibits nuclear import and promotes interaction with 14.3.3 proteins". Molecular and Cellular Biology. 22 (19): 6809–19. doi:10.1128/MCB.22.19.6809-6819.2002. PMC   134047 . PMID   12215538.

Further reading