Jump to content

MCM6: Difference between revisions

From Wikipedia, the free encyclopedia
Content deleted Content added
+ref linked to lactose? <reF>https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401057/</reF> Lactose intolerance: diagnosis, genetic, and clinical factors 2012
m Journal cites:, added 3 DOIs, added 1 PMID, added 1 PMC, templated 1 journal cites
Line 14: Line 14:
''MCM6'' contains two of the regulatory regions for [[Lactase|''LCT'']], the gene encoding the protein [[lactase]], located in two of the ''MCM6'' introns, approximately 14 kb (-13910) and 22 kb (-22018) upstream of ''LCT''.<ref name="Enattah_2002">{{cite journal | vauthors = Enattah NS, Sahi T, Savilahti E, Terwilliger JD, Peltonen L, Järvelä I | title = Identification of a variant associated with adult-type hypolactasia | journal = Nat. Genet. | volume = 30 | issue = 2 | pages = 233–7 | date = February 2002 | pmid = 11788828 | doi = 10.1038/ng826 }}</ref> The (-13910) region, in particular, has been shown to function ''in vitro'' as an [[Enhancer (genetics)|enhancer]] element capable of differentially activating transcription of ''LCT'' [[Promoter (biology)|promoter]].<ref name="pmid12915462">{{cite journal | vauthors = Olds LC, Sibley E | title = Lactase persistence DNA variant enhances lactase promoter activity in vitro: functional role as a cis regulatory element | journal = Hum. Mol. Genet. | volume = 12 | issue = 18 | pages = 2333–40 | date = September 2003 | pmid = 12915462 | doi = 10.1093/hmg/ddg244 }}</ref>
''MCM6'' contains two of the regulatory regions for [[Lactase|''LCT'']], the gene encoding the protein [[lactase]], located in two of the ''MCM6'' introns, approximately 14 kb (-13910) and 22 kb (-22018) upstream of ''LCT''.<ref name="Enattah_2002">{{cite journal | vauthors = Enattah NS, Sahi T, Savilahti E, Terwilliger JD, Peltonen L, Järvelä I | title = Identification of a variant associated with adult-type hypolactasia | journal = Nat. Genet. | volume = 30 | issue = 2 | pages = 233–7 | date = February 2002 | pmid = 11788828 | doi = 10.1038/ng826 }}</ref> The (-13910) region, in particular, has been shown to function ''in vitro'' as an [[Enhancer (genetics)|enhancer]] element capable of differentially activating transcription of ''LCT'' [[Promoter (biology)|promoter]].<ref name="pmid12915462">{{cite journal | vauthors = Olds LC, Sibley E | title = Lactase persistence DNA variant enhances lactase promoter activity in vitro: functional role as a cis regulatory element | journal = Hum. Mol. Genet. | volume = 12 | issue = 18 | pages = 2333–40 | date = September 2003 | pmid = 12915462 | doi = 10.1093/hmg/ddg244 }}</ref>


[[Mutation]]s in these regions are associated with [[lactose tolerance]] into adult life.<ref name="Enattah_2002"/><reF>[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401057/ Lactose intolerance: diagnosis, genetic, and clinical factors], Clin Exp Gastroenterol. 2012; 5: 113–121. [[doi:10.2147/CEG.S32368]] " Two variants were associated with lactase persistence..."</reF>
[[Mutation]]s in these regions are associated with [[lactose tolerance]] into adult life.<ref name="Enattah_2002"/><reF>{{cite journal | pmc = 3401057 |doi=10.2147/CEG.S32368 | pmid=22826639 | volume=5 | title=Lactose intolerance: diagnosis, genetic, and clinical factors | year=2012 | journal=Clin Exp Gastroenterol | pages=113–21 | vauthors=Mattar R, de Campos Mazo DF, Carrilho FJ}} " Two variants were associated with lactase persistence..."</reF>


== Interactions ==
== Interactions ==
Line 21: Line 21:
{{div col|colwidth=20em}}
{{div col|colwidth=20em}}
* [[CDC45-related protein]],<ref name = pmid12614612/>
* [[CDC45-related protein]],<ref name = pmid12614612/>
* [[MCM2]],<ref name = pmid12614612/><ref name = pmid12694531/><ref name = pmid12207017/><ref name = "pmid16189514">{{cite journal | vauthors = Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M | title = Towards a proteome-scale map of the human protein-protein interaction network | journal = Nature | volume = 437 | issue = 7062 | pages = 1173–8 | date = October 2005 | pmid = 16189514 | doi = 10.1038/nature04209 }}</ref><ref name = "pmid10567526">{{cite journal | vauthors = You Z, Komamura Y, Ishimi Y | title = Biochemical analysis of the intrinsic Mcm4-Mcm6-mcm7 DNA helicase activity | journal = Mol. Cell. Biol. | volume = 19 | issue = 12 | pages = 8003–15 | date = December 1999 | pmid = 10567526 | pmc = 84885 | doi = }}</ref>
* [[MCM2]],<ref name = pmid12614612/><ref name = pmid12694531/><ref name = pmid12207017/><ref name = "pmid16189514">{{cite journal | vauthors = Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M | title = Towards a proteome-scale map of the human protein-protein interaction network | journal = Nature | volume = 437 | issue = 7062 | pages = 1173–8 | date = October 2005 | pmid = 16189514 | doi = 10.1038/nature04209 }}</ref><ref name = "pmid10567526">{{cite journal | vauthors = You Z, Komamura Y, Ishimi Y | title = Biochemical analysis of the intrinsic Mcm4-Mcm6-mcm7 DNA helicase activity | journal = Mol. Cell. Biol. | volume = 19 | issue = 12 | pages = 8003–15 | date = December 1999 | pmid = 10567526 | pmc = 84885 | doi = 10.1128/MCB.19.12.8003}}</ref>
* [[MCM4]],<ref name = "pmid12694531">{{cite journal | vauthors = Yabuta N, Kajimura N, Mayanagi K, Sato M, Gotow T, Uchiyama Y, Ishimi Y, Nojima H | title = Mammalian Mcm2/4/6/7 complex forms a toroidal structure | journal = Genes Cells | volume = 8 | issue = 5 | pages = 413–21 | date = May 2003 | pmid = 12694531 | doi = 10.1046/j.1365-2443.2003.00645.x}}</ref><ref name = "pmid12207017">{{cite journal | vauthors = You Z, Ishimi Y, Masai H, Hanaoka F | title = Roles of Mcm7 and Mcm4 subunits in the DNA helicase activity of the mouse Mcm4/6/7 complex | journal = J. Biol. Chem. | volume = 277 | issue = 45 | pages = 42471–9 | date = November 2002 | pmid = 12207017 | doi = 10.1074/jbc.M205769200 }}</ref><ref name = "pmid8798650">{{cite journal | vauthors = Ishimi Y, Ichinose S, Omori A, Sato K, Kimura H | title = Binding of human minichromosome maintenance proteins with histone H3 | journal = J. Biol. Chem. | volume = 271 | issue = 39 | pages = 24115–22 | date = September 1996 | pmid = 8798650 | doi = 10.1074/jbc.271.39.24115}}</ref>
* [[MCM4]],<ref name = "pmid12694531">{{cite journal | vauthors = Yabuta N, Kajimura N, Mayanagi K, Sato M, Gotow T, Uchiyama Y, Ishimi Y, Nojima H | title = Mammalian Mcm2/4/6/7 complex forms a toroidal structure | journal = Genes Cells | volume = 8 | issue = 5 | pages = 413–21 | date = May 2003 | pmid = 12694531 | doi = 10.1046/j.1365-2443.2003.00645.x}}</ref><ref name = "pmid12207017">{{cite journal | vauthors = You Z, Ishimi Y, Masai H, Hanaoka F | title = Roles of Mcm7 and Mcm4 subunits in the DNA helicase activity of the mouse Mcm4/6/7 complex | journal = J. Biol. Chem. | volume = 277 | issue = 45 | pages = 42471–9 | date = November 2002 | pmid = 12207017 | doi = 10.1074/jbc.M205769200 }}</ref><ref name = "pmid8798650">{{cite journal | vauthors = Ishimi Y, Ichinose S, Omori A, Sato K, Kimura H | title = Binding of human minichromosome maintenance proteins with histone H3 | journal = J. Biol. Chem. | volume = 271 | issue = 39 | pages = 24115–22 | date = September 1996 | pmid = 8798650 | doi = 10.1074/jbc.271.39.24115}}</ref>
* [[MCM7]],<ref name = pmid12207017/><ref name = "pmid9099751">{{cite journal | vauthors = Fujita M, Kiyono T, Hayashi Y, Ishibashi M | title = In vivo interaction of human MCM heterohexameric complexes with chromatin. Possible involvement of ATP | journal = J. Biol. Chem. | volume = 272 | issue = 16 | pages = 10928–35 | date = April 1997 | pmid = 9099751 | doi = 10.1074/jbc.272.16.10928}}</ref>
* [[MCM7]],<ref name = pmid12207017/><ref name = "pmid9099751">{{cite journal | vauthors = Fujita M, Kiyono T, Hayashi Y, Ishibashi M | title = In vivo interaction of human MCM heterohexameric complexes with chromatin. Possible involvement of ATP | journal = J. Biol. Chem. | volume = 272 | issue = 16 | pages = 10928–35 | date = April 1997 | pmid = 9099751 | doi = 10.1074/jbc.272.16.10928}}</ref>
Line 44: Line 44:
* {{cite journal | vauthors = Holthoff HP, Baack M, Richter A, Ritzi M, Knippers R | title = Human protein MCM6 on HeLa cell chromatin | journal = J. Biol. Chem. | volume = 273 | issue = 13 | pages = 7320–5 | year = 1998 | pmid = 9516426 | doi = 10.1074/jbc.273.13.7320 }}
* {{cite journal | vauthors = Holthoff HP, Baack M, Richter A, Ritzi M, Knippers R | title = Human protein MCM6 on HeLa cell chromatin | journal = J. Biol. Chem. | volume = 273 | issue = 13 | pages = 7320–5 | year = 1998 | pmid = 9516426 | doi = 10.1074/jbc.273.13.7320 }}
* {{cite journal | vauthors = Ohtani K, Iwanaga R, Nakamura M, Ikeda M, Yabuta N, Tsuruga H, Nojima H | title = Cell growth-regulated expression of mammalian MCM5 and MCM6 genes mediated by the transcription factor E2F | journal = Oncogene | volume = 18 | issue = 14 | pages = 2299–309 | year = 1999 | pmid = 10327050 | doi = 10.1038/sj.onc.1202544 }}
* {{cite journal | vauthors = Ohtani K, Iwanaga R, Nakamura M, Ikeda M, Yabuta N, Tsuruga H, Nojima H | title = Cell growth-regulated expression of mammalian MCM5 and MCM6 genes mediated by the transcription factor E2F | journal = Oncogene | volume = 18 | issue = 14 | pages = 2299–309 | year = 1999 | pmid = 10327050 | doi = 10.1038/sj.onc.1202544 }}
* {{cite journal | vauthors = You Z, Komamura Y, Ishimi Y | title = Biochemical analysis of the intrinsic Mcm4-Mcm6-mcm7 DNA helicase activity | journal = Mol. Cell. Biol. | volume = 19 | issue = 12 | pages = 8003–15 | year = 2000 | pmid = 10567526 | pmc = 84885 | doi = }}
* {{cite journal | vauthors = You Z, Komamura Y, Ishimi Y | title = Biochemical analysis of the intrinsic Mcm4-Mcm6-mcm7 DNA helicase activity | journal = Mol. Cell. Biol. | volume = 19 | issue = 12 | pages = 8003–15 | year = 2000 | pmid = 10567526 | pmc = 84885 | doi = 10.1128/MCB.19.12.8003}}
* {{cite journal | vauthors = Ishimi Y, Komamura-Kohno Y, You Z, Omori A, Kitagawa M | title = Inhibition of Mcm4,6,7 helicase activity by phosphorylation with cyclin A/Cdk2 | journal = J. Biol. Chem. | volume = 275 | issue = 21 | pages = 16235–41 | year = 2000 | pmid = 10748114 | doi = 10.1074/jbc.M909040199 }}
* {{cite journal | vauthors = Ishimi Y, Komamura-Kohno Y, You Z, Omori A, Kitagawa M | title = Inhibition of Mcm4,6,7 helicase activity by phosphorylation with cyclin A/Cdk2 | journal = J. Biol. Chem. | volume = 275 | issue = 21 | pages = 16235–41 | year = 2000 | pmid = 10748114 | doi = 10.1074/jbc.M909040199 }}
* {{cite journal | vauthors = Izumi M, Yanagi K, Mizuno T, Yokoi M, Kawasaki Y, Moon KY, Hurwitz J, Yatagai F, Hanaoka F | title = The human homolog of Saccharomyces cerevisiae Mcm10 interacts with replication factors and dissociates from nuclease-resistant nuclear structures in G(2) phase | journal = Nucleic Acids Res. | volume = 28 | issue = 23 | pages = 4769–77 | year = 2001 | pmid = 11095689 | pmc = 115166 | doi = 10.1093/nar/28.23.4769 }}
* {{cite journal | vauthors = Izumi M, Yanagi K, Mizuno T, Yokoi M, Kawasaki Y, Moon KY, Hurwitz J, Yatagai F, Hanaoka F | title = The human homolog of Saccharomyces cerevisiae Mcm10 interacts with replication factors and dissociates from nuclease-resistant nuclear structures in G(2) phase | journal = Nucleic Acids Res. | volume = 28 | issue = 23 | pages = 4769–77 | year = 2001 | pmid = 11095689 | pmc = 115166 | doi = 10.1093/nar/28.23.4769 }}

Revision as of 13:42, 16 November 2019

MCM6
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesMCM6, MCG40308, Mis5, P105MCM, minichromosome maintenance complex component 6
External IDsOMIM: 601806; MGI: 1298227; HomoloGene: 4322; GeneCards: MCM6; OMA:MCM6 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005915

NM_008567
NM_001313695

RefSeq (protein)

NP_005906

NP_001300624
NP_032593

Location (UCSC)Chr 2: 135.84 – 135.88 MbChr 1: 128.26 – 128.29 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

DNA replication licensing factor MCM6 is a protein that in humans is encoded by the MCM6 gene.[5] MCM6 is one of the highly conserved mini-chromosome maintenance proteins (MCM) that are essential for the initiation of eukaryotic genome replication.

Function

The MCM complex consisting of MCM6 (this protein) and MCM2, 4 and 7 possesses DNA helicase activity, and may act as a DNA unwinding enzyme. The hexameric protein complex formed by the MCM proteins is a key component of the pre-replication complex (pre-RC) and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. The phosphorylation of the complex by CDC2 kinase reduces the helicase activity, suggesting a role in the regulation of DNA replication.[6] Mcm 6 has recently been shown to interact strongly Cdt1 at defined residues, by mutating these target residues Wei et al. observed lack of Cdt1 recruitment of Mcm2-7 to the pre-RC.[7]

Gene

The MCM6 gene, MCM6, is expressed at very high level. MCM6 contains 18 introns. There are 2 non overlapping alternative last exons. The transcripts appear to differ by truncation of the 3' end, presence or absence of 2 cassette exons, common exons with different boundaries.

MCM6 produces, by alternative splicing, 3 different transcripts, all with introns, putatively encoding 3 different protein isoforms.

MCM6 contains two of the regulatory regions for LCT, the gene encoding the protein lactase, located in two of the MCM6 introns, approximately 14 kb (-13910) and 22 kb (-22018) upstream of LCT.[8] The (-13910) region, in particular, has been shown to function in vitro as an enhancer element capable of differentially activating transcription of LCT promoter.[9]

Mutations in these regions are associated with lactose tolerance into adult life.[8][10]

Interactions

MCM6 has been shown to interact with:

See also

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000076003Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000026355Ensembl, 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. ^ Harvey CB, Wang Y, Darmoul D, Phillips A, Mantei N, Swallow DM (December 1996). "Characterisation of a human homologue of a yeast cell division cycle gene, MCM6, located adjacent to the 5' end of the lactase gene on chromosome 2q21". FEBS Lett. 398 (2–3): 135–40. doi:10.1016/S0014-5793(96)01189-1. PMID 8977093.
  6. ^ "Entrez Gene: MCM6 minichromosome maintenance deficient 6 homolog (S. cerevisiae)".
  7. ^ Wei Z, Liu C, Wu X, Xu N, Zhou B, Liang C, Zhu G (March 2010). "Characterization and structure determination of the Cdt1 binding domain of human minichromosome maintenance (Mcm) 6". J Biol Chem. 285 (17): 12469–73. doi:10.1074/jbc.C109.094599. PMC 2857124. PMID 20202939.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  8. ^ a b Enattah NS, Sahi T, Savilahti E, Terwilliger JD, Peltonen L, Järvelä I (February 2002). "Identification of a variant associated with adult-type hypolactasia". Nat. Genet. 30 (2): 233–7. doi:10.1038/ng826. PMID 11788828.
  9. ^ Olds LC, Sibley E (September 2003). "Lactase persistence DNA variant enhances lactase promoter activity in vitro: functional role as a cis regulatory element". Hum. Mol. Genet. 12 (18): 2333–40. doi:10.1093/hmg/ddg244. PMID 12915462.
  10. ^ Mattar R, de Campos Mazo DF, Carrilho FJ (2012). "Lactose intolerance: diagnosis, genetic, and clinical factors". Clin Exp Gastroenterol. 5: 113–21. doi:10.2147/CEG.S32368. PMC 3401057. PMID 22826639.{{cite journal}}: CS1 maint: unflagged free DOI (link) " Two variants were associated with lactase persistence..."
  11. ^ a b c d e f Kneissl M, Pütter V, Szalay AA, Grummt F (March 2003). "Interaction and assembly of murine pre-replicative complex proteins in yeast and mouse cells". J. Mol. Biol. 327 (1): 111–28. doi:10.1016/s0022-2836(03)00079-2. PMID 12614612.
  12. ^ a b Yabuta N, Kajimura N, Mayanagi K, Sato M, Gotow T, Uchiyama Y, Ishimi Y, Nojima H (May 2003). "Mammalian Mcm2/4/6/7 complex forms a toroidal structure". Genes Cells. 8 (5): 413–21. doi:10.1046/j.1365-2443.2003.00645.x. PMID 12694531.
  13. ^ a b c You Z, Ishimi Y, Masai H, Hanaoka F (November 2002). "Roles of Mcm7 and Mcm4 subunits in the DNA helicase activity of the mouse Mcm4/6/7 complex". J. Biol. Chem. 277 (45): 42471–9. doi:10.1074/jbc.M205769200. PMID 12207017.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  14. ^ Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M (October 2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.
  15. ^ You Z, Komamura Y, Ishimi Y (December 1999). "Biochemical analysis of the intrinsic Mcm4-Mcm6-mcm7 DNA helicase activity". Mol. Cell. Biol. 19 (12): 8003–15. doi:10.1128/MCB.19.12.8003. PMC 84885. PMID 10567526.
  16. ^ Ishimi Y, Ichinose S, Omori A, Sato K, Kimura H (September 1996). "Binding of human minichromosome maintenance proteins with histone H3". J. Biol. Chem. 271 (39): 24115–22. doi:10.1074/jbc.271.39.24115. PMID 8798650.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  17. ^ Fujita M, Kiyono T, Hayashi Y, Ishibashi M (April 1997). "In vivo interaction of human MCM heterohexameric complexes with chromatin. Possible involvement of ATP". J. Biol. Chem. 272 (16): 10928–35. doi:10.1074/jbc.272.16.10928. PMID 9099751.{{cite journal}}: CS1 maint: unflagged free DOI (link)

Further reading