ZFY: Difference between revisions

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Importing Wikidata short description: "Protein-coding gene in the species Homo sapiens" (Shortdesc helper)
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This gene encodes a [[zinc finger]]-containing protein that may function as a [[transcription factor]]. This gene was once a candidate gene for the [[testis-determining factor]] (TDF) and was erroneously referred to as TDF.<ref name="entrez" />
This gene encodes a [[zinc finger]]-containing protein that may function as a [[transcription factor]]. This gene was once a candidate gene for the [[testis-determining factor]] (TDF) and was erroneously referred to as TDF.<ref name="entrez" />


Humans express a single ZFY gene with two [[alternative splicing|splice variants]]. While mice express two [[sequence homology|paralogous]] copies, Zfy1 and Zfy2.<ref name="Vernet_2016">{{cite journal | vauthors = Vernet N, Mahadevaiah SK, de Rooij DG, Burgoyne PS, Ellis PJ | title = Zfy genes are required for efficient meiotic sex chromosome inactivation (MSCI) in spermatocytes | journal = Human Molecular Genetics | volume = 25 | issue = 24 | pages = 5300–5310 | date = December 2016 | pmid = 27742779 | pmc = 5418838 | doi = 10.1093/hmg/ddw344 }}</ref> During [[spermatogenesis]], wrongful expression of either Zfy1 or Zfy2 results in programmed cell death, [[apoptosis]], at the [[meiosis|mid-pachytene]] checkpoint. In mice, Zfy genes are necessary for meiotic sex chromosome inactivation (MSCI). In Zfy knockout spermatocytes, sex chromosomes are incorrectly silenced. Thus, Zfy performs three functions at the mid-pachytene checkpoint: (1) promote MSCI, (2) monitor MSCI progress, and (3) execute cells, via apoptosis, that fail to undergo MSCI.<ref name="Vernet_2016" />
Humans express a single ZFY gene with two [[alternative splicing|splice variants]], while mice express two [[sequence homology|paralogous]] copies, Zfy1 and Zfy2.<ref name="Vernet_2016">{{cite journal | vauthors = Vernet N, Mahadevaiah SK, de Rooij DG, Burgoyne PS, Ellis PJ | title = Zfy genes are required for efficient meiotic sex chromosome inactivation (MSCI) in spermatocytes | journal = Human Molecular Genetics | volume = 25 | issue = 24 | pages = 5300–5310 | date = December 2016 | pmid = 27742779 | pmc = 5418838 | doi = 10.1093/hmg/ddw344 }}</ref> During [[spermatogenesis]], wrongful expression of either Zfy1 or Zfy2 results in programmed cell death, [[apoptosis]], at the [[meiosis|mid-pachytene]] checkpoint. In mice, Zfy genes are necessary for meiotic sex chromosome inactivation (MSCI). In Zfy knockout spermatocytes, sex chromosomes are incorrectly silenced. Thus, Zfy performs three functions at the mid-pachytene checkpoint: (1) promote MSCI, (2) monitor MSCI progress, and (3) execute cells, via apoptosis, that fail to undergo MSCI.<ref name="Vernet_2016" />


In humans, ZFY is most broadly expresses in the testis and prostate. However, 20 other tissues also express ZFY, such as esophagus, urinary bladder, bone marrow, small intestine, appendix and gall bladder.<ref>{{cite web | title = ZFY Gene |url= https://www.genecards.org/cgi-bin/carddisp.pl?gene=ZFY#expression | work = GeneCards |access-date=2019-04-15}}</ref>
In humans, ZFY is most broadly expresses in the testis and prostate. However, 20 other tissues also express ZFY, such as esophagus, urinary bladder, bone marrow, small intestine, appendix and gall bladder.<ref>{{cite web | title = ZFY Gene |url= https://www.genecards.org/cgi-bin/carddisp.pl?gene=ZFY#expression | work = GeneCards |access-date=2019-04-15}}</ref>
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{{refbegin | 2}}
{{refbegin | 2}}
* {{cite journal | vauthors = Merchant-Larios H, Moreno-Mendoza N | title = Onset of sex differentiation: dialog between genes and cells | journal = Archives of Medical Research | volume = 32 | issue = 6 | pages = 553–8 | year = 2002 | pmid = 11750730 | doi = 10.1016/S0188-4409(01)00317-4 }}
* {{cite journal | vauthors = Merchant-Larios H, Moreno-Mendoza N | title = Onset of sex differentiation: dialog between genes and cells | journal = Archives of Medical Research | volume = 32 | issue = 6 | pages = 553–8 | year = 2002 | pmid = 11750730 | doi = 10.1016/S0188-4409(01)00317-4 }}
* {{cite journal | vauthors = Kochoyan M, Havel TF, Nguyen DT, Dahl CE, Keutmann HT, Weiss MA | title = Alternating zinc fingers in the human male associated protein ZFY: 2D NMR structure of an even finger and implications for "jumping-linker" DNA recognition | journal = Biochemistry | volume = 30 | issue = 14 | pages = 3371–86 | date = April 1991 | pmid = 1849423 | doi = 10.1021/bi00228a004 }}
* {{cite journal | vauthors = Kochoyan M, Havel TF, Nguyen DT, Dahl CE, Keutmann HT, Weiss MA | title = Alternating zinc fingers in the human male associated protein ZFY: 2D NMR structure of an even finger and implications for "jumping-linker" DNA recognition | journal = Biochemistry | volume = 30 | issue = 14 | pages = 3371–86 | date = April 1991 | pmid = 1849423 | doi = 10.1021/bi00228a004 | s2cid = 24544613 }}
* {{cite journal | vauthors = Kochoyan M, Keutmann HT, Weiss MA | title = Alternating zinc fingers in the human male associated protein ZFY: refinement of the NMR structure of an even finger by selective deuterium labeling and implications for DNA recognition | journal = Biochemistry | volume = 30 | issue = 29 | pages = 7063–72 | date = July 1991 | pmid = 1854720 | doi = 10.1021/bi00243a005 }}
* {{cite journal | vauthors = Kochoyan M, Keutmann HT, Weiss MA | title = Alternating zinc fingers in the human male associated protein ZFY: refinement of the NMR structure of an even finger by selective deuterium labeling and implications for DNA recognition | journal = Biochemistry | volume = 30 | issue = 29 | pages = 7063–72 | date = July 1991 | pmid = 1854720 | doi = 10.1021/bi00243a005 }}
* {{cite journal | vauthors = North M, Sargent C, O'Brien J, Taylor K, Wolfe J, Affara NA, Ferguson-Smith MA | title = Comparison of ZFY and ZFX gene structure and analysis of alternative 3' untranslated regions of ZFY | journal = Nucleic Acids Research | volume = 19 | issue = 10 | pages = 2579–86 | date = May 1991 | pmid = 2041734 | pmc = 328173 | doi = 10.1093/nar/19.10.2579 }}
* {{cite journal | vauthors = North M, Sargent C, O'Brien J, Taylor K, Wolfe J, Affara NA, Ferguson-Smith MA | title = Comparison of ZFY and ZFX gene structure and analysis of alternative 3' untranslated regions of ZFY | journal = Nucleic Acids Research | volume = 19 | issue = 10 | pages = 2579–86 | date = May 1991 | pmid = 2041734 | pmc = 328173 | doi = 10.1093/nar/19.10.2579 }}

Latest revision as of 13:40, 18 December 2023

ZFY
Available structures
PDBHuman UniProt search: PDBe RCSB
Identifiers
AliasesZFY, ZNF911, zinc finger protein, Y-linked, zinc finger protein Y-linked
External IDsOMIM: 490000 HomoloGene: 88465 GeneCards: ZFY
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001145275
NM_001145276
NM_003411

n/a

RefSeq (protein)

n/a

Location (UCSC)Chr Y: 2.94 – 2.98 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

Zinc finger Y-chromosomal protein is a protein that in humans is encoded by the ZFY gene of the Y chromosome.[3][4]

This gene encodes a zinc finger-containing protein that may function as a transcription factor. This gene was once a candidate gene for the testis-determining factor (TDF) and was erroneously referred to as TDF.[4]

Humans express a single ZFY gene with two splice variants, while mice express two paralogous copies, Zfy1 and Zfy2.[5] During spermatogenesis, wrongful expression of either Zfy1 or Zfy2 results in programmed cell death, apoptosis, at the mid-pachytene checkpoint. In mice, Zfy genes are necessary for meiotic sex chromosome inactivation (MSCI). In Zfy knockout spermatocytes, sex chromosomes are incorrectly silenced. Thus, Zfy performs three functions at the mid-pachytene checkpoint: (1) promote MSCI, (2) monitor MSCI progress, and (3) execute cells, via apoptosis, that fail to undergo MSCI.[5]

In humans, ZFY is most broadly expresses in the testis and prostate. However, 20 other tissues also express ZFY, such as esophagus, urinary bladder, bone marrow, small intestine, appendix and gall bladder.[6]

Disorders associated with the ZFY gene include campomelic dysplasia, cystadenofibroma, and Frasier syndrome.[7]

References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000067646Ensembl, May 2017
  2. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. ^ Müller G, Schempp W (April 1989). "Mapping the human ZFX locus to Xp21.3 by in situ hybridization". Human Genetics. 82 (1): 82–4. doi:10.1007/BF00288279. PMID 2497060. S2CID 27908892.
  4. ^ a b "Entrez Gene: ZFY zinc finger protein, Y-linked".
  5. ^ a b Vernet N, Mahadevaiah SK, de Rooij DG, Burgoyne PS, Ellis PJ (December 2016). "Zfy genes are required for efficient meiotic sex chromosome inactivation (MSCI) in spermatocytes". Human Molecular Genetics. 25 (24): 5300–5310. doi:10.1093/hmg/ddw344. PMC 5418838. PMID 27742779.
  6. ^ "ZFY Gene". GeneCards. Retrieved 2019-04-15.
  7. ^ "MalaCards: Search Human Diseases - ZFY". Mala Cards. Retrieved 2019-04-15.

Further reading[edit]