ZXDC

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ZXDC
Identifiers
AliasesZXDC, ZXDL, ZXD family zinc finger C
External IDsOMIM: 615746 MGI: 1933108 HomoloGene: 82340 GeneCards: ZXDC
Orthologs
SpeciesHumanMouse
Entrez

79364

80292

Ensembl

ENSG00000070476

ENSMUSG00000034430

UniProt

Q2QGD7

Q8C8V1

RefSeq (mRNA)

NM_001040653
NM_025112

NM_030260
NM_173002

RefSeq (protein)

NP_001035743
NP_079388

NP_084536
NP_766590

Location (UCSC)Chr 3: 126.44 – 126.48 MbChr 6: 90.35 – 90.38 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Zinc finger, X-linked, duplicated family member C (ZXDC) is a human CIITA-binding protein involved in the activation of major histocompatibility complex (MHC) class I and II.[5] For binding to occur, ZXDC must form an oligomeric complex with another copy of itself or with ZXDA, a related protein.[6] ZXDC is activated by sumoylation, a post-translational modification.[7] ZXDC plays a role in controlling immunological responses, cancer formation and progression, and cell proliferation, differentiation, and survival.

History[edit]

When Sakaue and colleagues searched for novel transcription factors involved in the development of Xenopus laevis, they discovered ZXDC (ZXD Family Zinc Finger C). This discovery was discovered in a research article that was published in 1998. They found a cDNA clone called "Xfin" that encodes a protein with two zinc finger C2H2 domains.[8]

Later research established the interspecies conservation of the Xfin protein, and the human equivalent was given the name ZXDC. It was discovered that the protein was broadly generated in human tissues and that a number of variables, including hypoxia, estrogen, and cytokines, controlled how the protein was expressed.

Structure[edit]

ZXDC is a protein composed of 455 amino acids in humans, with a molecular weight of approximately 49.9 kDa.

Near its C-terminus, the protein has two C2H2-type zinc finger domains that are likely to be involved in DNA binding and transcriptional control. A flexible linker region that separates the zinc fingers may provide more adaptability in binding to various DNA sequences.

Other domains found in ZXDC include a proline-rich region close to the N-terminus that may be important in protein-protein interactions and a central region that is projected to be intrinsically disordered. ZXDC also contains numerous other features in addition to the zinc fingers. Although the exact purpose of these domains is not yet known, they might assist in mediating interactions with other proteins or controlling the activity of the protein.[9]

ZXDC has mostly been investigated in the context of developmental biology and cell fate determination in animals. Studies in fruit flies, for instance, have demonstrated that protein is crucial for the development of particular cell types, such as the cell precursors of the sensory organs in the peripheral nervous system.[10]

Function[edit]

ZXDC is highly conserved between species, showing the significance of this gene for cellular function. ZXDC is a member of the zinc finger family of proteins that are crucial for the regulation of genes and cellular functions in a variety of organisms.

ZXDC (ZXD Family Zinc Finger C) is a protein-coding gene that controls biological processes such as cell division, proliferation, and apoptosis. This gene produces a protein with two C2H2-type zinc fingers that are a member of the ZXD family.[11]

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ZXDC has been linked to the formation of numerous cancer forms and it regulates the advancement of the cell cycle. It is also known to interact with other proteins, including GSK3β, a serine/threonine protein kinase implicated in a number of signaling pathways, and p53, an important tumor suppressor.[12]

By regulating the expression of genes linked to the innate immune response, ZXDC has also been demonstrated to contribute to the regulation of immunological responses. As a result, it is believed that ZXDC could be a possible target for the creation of new remedies for autoimmune and cancerous conditions.[13]

ZXDC is involved in controlling the circadian clock in cells, which regulates the daily cycles of physiological processes.[citation needed]

Isolation[edit]

ZXDC's solubility is not well described in the literature and may vary depending on a number of variables, including the protein's expression system, the buffering situation, and the presence of other proteins or chemicals. But studies have shown the effective separation of ZXDC using a variety of techniques, including gel filtration and affinity chromatography, suggesting that the protein is probably soluble in some circumstances. For instance, one study found superior amounts of soluble protein and pure recombinant ZXDC protein generated in Escherichia Coli using immobilized metal affinity chromatography (IMAC).[14]

Role in disease[edit]

Numerous cancers, including breast, lung, and colorectal cancer, have been linked to ZXDC, according to studies. It is also considered to be a possible therapeutic target for autoimmune and cancer conditions. ZXDC abnormality has been linked to cancer progression and an unfavorable prognosis.

In breast cancer, low ZXDC expression has been associated with tumor invasiveness, lymph node metastases, and poor prognosis. ZXDC suppresses the growth and migration of breast cancer cells, acting as a tumor suppressor.

The emergence of a more aggressive form of lung cancer has been correlated with decreased ZXDC expression. Studies have demonstrated that increasing ZXDC expression can prevent tumor development and invasion in lung cancer cells.[15]

In colorectal cancer, the loss of ZXDC expression has been connected to the advancement of the disease stage and lymph node metastasis. In addition, it has been proposed that ZXDC may function as a tumor suppressor by obstructing the Wnt/beta-catenin signaling pathway, which is frequently active in colorectal cancer.

Overall, these results indicate that ZXDC may be a key player in the initiation and development of cancer, and it may also hold interest as a diagnostic or therapeutic target for the treatment of cancer. To completely comprehend the processes underlying ZXDC's activity in cancer and to design specific treatments based on it, more study is necessary.[16]

References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000070476 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000034430 – 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. ^ Al-Kandari W, Jambunathan S, Navalgund V, Koneni R, Freer M, Parimi N, et al. (January 2007). "ZXDC, a novel zinc finger protein that binds CIITA and activates MHC gene transcription". Molecular Immunology. 44 (4): 311–321. doi:10.1016/j.molimm.2006.02.029. PMC 1624858. PMID 16600381.
  6. ^ Al-Kandari W, Koneni R, Navalgund V, Aleksandrova A, Jambunathan S, Fontes JD (June 2007). "The zinc finger proteins ZXDA and ZXDC form a complex that binds CIITA and regulates MHC II gene transcription". Journal of Molecular Biology. 369 (5): 1175–1187. doi:10.1016/j.jmb.2007.04.033. PMC 1963517. PMID 17493635.
  7. ^ Jambunathan S, Fontes JD (September 2007). "Sumoylation of the zinc finger protein ZXDC enhances the function of its transcriptional activation domain". Biological Chemistry. 388 (9): 965–972. doi:10.1515/BC.2007.106. PMID 17696781. S2CID 1007656.
  8. ^ Wargent ET, Martin-Gronert MS, Cripps RL, Heisler LK, Yeo GS, Ozanne SE, et al. (September 2020). "Developmental programming of appetite and growth in male rats increases hypothalamic serotonin (5-HT)5A receptor expression and sensitivity" (PDF). International Journal of Obesity. 44 (9): 1946–1957. doi:10.1038/s41366-020-0643-2. PMID 32719434. S2CID 220810612.
  9. ^ Al-Kandari W, Jambunathan S, Navalgund V, Koneni R, Freer M, Parimi N, et al. (January 2007). "ZXDC, a novel zinc finger protein that binds CIITA and activates MHC gene transcription". Molecular Immunology. 44 (4): 311–321. doi:10.1016/j.molimm.2006.02.029. PMC 1624858. PMID 16600381.
  10. ^ Seetharam A, Bai Y, Stuart GW (April 2010). "A survey of well conserved families of C2H2 zinc-finger genes in Daphnia". BMC Genomics. 11 (1): 276. doi:10.1186/1471-2164-11-276. PMC 2889900. PMID 20433734.
  11. ^ Ozturk S, Kosebent EG, Talibova G, Bilmez Y, Tire B, Can A (February 2023). "Embryonic poly(A)-binding protein interacts with translation-related proteins and undergoes phosphorylation on the serine, threonine, and tyrosine residues in the mouse oocytes and early embryos". Journal of Assisted Reproduction and Genetics. 40 (4): 929–941. doi:10.1007/s10815-023-02746-7. PMC 10224904. PMID 36823316. S2CID 257153864.
  12. ^ Bellanné-Chantelot C, Rabadan Moraes G, Schmaltz-Panneau B, Marty C, Vainchenker W, Plo I (July 2020). "Germline genetic factors in the pathogenesis of myeloproliferative neoplasms" (PDF). Blood Reviews. 42: 100710. doi:10.1016/j.blre.2020.100710. PMID 32532454. S2CID 219620040.
  13. ^ Ollila H, Wennerstrom A, Partinen M, Mignot E, Saarela J, Saavalainen P, Vaarala O, Tienari P, Perola M (January 2019). "Genetics of vaccination-related narcolepsy". European Neuropsychopharmacology. 29: S994. bioRxiv 10.1101/169623. doi:10.1016/j.euroneuro.2017.08.379. S2CID 90650123.
  14. ^ Takenawa T, Kuramitsu Y, Wang Y, Okada F, Tokuda K, Kitagawa T, et al. (January 2013). "Proteomic analysis showed down-regulation of nucleophosmin in progressive tumor cells compared to regressive tumor cells". Anticancer Research. 33 (1): 153–160. PMID 23267140.
  15. ^ Hu J, Chen Z, Bao L, Zhou L, Hou Y, Liu L, et al. (July 2020). "Single-Cell Transcriptome Analysis Reveals Intratumoral Heterogeneity in ccRCC, which Results in Different Clinical Outcomes". Molecular Therapy. 28 (7): 1658–1672. doi:10.1016/j.ymthe.2020.04.023. PMC 7335756. PMID 32396851.
  16. ^ O'Farrell HE, Bowman RV, Fong KM, Yang IA (May 2021). "Plasma Extracellular Vesicle miRNAs Can Identify Lung Cancer, Current Smoking Status, and Stable COPD". International Journal of Molecular Sciences. 22 (11): 5803. doi:10.3390/ijms22115803. PMC 8198071. PMID 34071592.

External links[edit]

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