MSH5: Difference between revisions

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<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{Infobox_gene}}
{{PBB_Controls
'''MutS protein homolog 5''' is a [[protein]] that in humans is encoded by the ''MSH5'' [[gene]].<ref name="pmid9740671">{{cite journal | vauthors = Her C, Doggett NA | title = Cloning, structural characterization, and chromosomal localization of the human orthologue of Saccharomyces cerevisiae MSH5 gene | journal = Genomics | volume = 52 | issue = 1 | pages = 50–61 | date = Aug 1998 | pmid = 9740671 | pmc =  | doi = 10.1006/geno.1998.5374 }}</ref><ref name="pmid9787078">{{cite journal | vauthors = Winand NJ, Panzer JA, Kolodner RD | title = Cloning and characterization of the human and Caenorhabditis elegans homologs of the Saccharomyces cerevisiae MSH5 gene | journal = Genomics | volume = 53 | issue = 1 | pages = 69–80 | date = Oct 1998 | pmid = 9787078 | pmc =  | doi = 10.1006/geno.1998.5447 }}</ref><ref name="pmid17977839">{{cite journal | vauthors = Snowden T, Shim KS, Schmutte C, Acharya S, Fishel R | title = hMSH4-hMSH5 adenosine nucleotide processing and interactions with homologous recombination machinery | journal = The Journal of Biological Chemistry | volume = 283 | issue = 1 | pages = 145–54 | date = Jan 2008 | pmid = 17977839 | pmc = 2841433 | doi = 10.1074/jbc.M704060200 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: MSH5 mutS homolog 5 (E. coli)| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4439| accessdate = }}</ref>
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
}}


<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
== Function ==
{{GNF_Protein_box
| image =
| image_source =
| PDB =
| Name = MutS homolog 5 (E. coli)
| HGNCid = 7328
| Symbol = MSH5
| AltSymbols =; DKFZp434C1615; G7; MGC2939; MutSH5; NG23
| OMIM = 603382
| ECnumber = 
| Homologene = 8415
| MGIid = 1329021
| GeneAtlas_image1 = PBB_GE_MSH5_210410_s_at_tn.png
| GeneAtlas_image2 = PBB_GE_MSH5_221406_s_at_tn.png
| GeneAtlas_image3 = PBB_GE_MSH5_212913_at_tn.png
| Function = {{GNF_GO|id=GO:0000166 |text = nucleotide binding}} {{GNF_GO|id=GO:0003684 |text = damaged DNA binding}} {{GNF_GO|id=GO:0005524 |text = ATP binding}}
| Component =
| Process = {{GNF_GO|id=GO:0006259 |text = DNA metabolic process}} {{GNF_GO|id=GO:0006298 |text = mismatch repair}} {{GNF_GO|id=GO:0007126 |text = meiosis}} {{GNF_GO|id=GO:0007131 |text = meiotic recombination}} {{GNF_GO|id=GO:0007136 |text = meiotic prophase II}}
| Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 4439
    | Hs_Ensembl = ENSG00000096474
    | Hs_RefseqProtein = XP_001131770
    | Hs_RefseqmRNA = XM_001131770
    | Hs_GenLoc_db = 
    | Hs_GenLoc_chr = c6_COX
    | Hs_GenLoc_start = 31842436
    | Hs_GenLoc_end = 31867259
    | Hs_Uniprot = Q5SSQ6
    | Mm_EntrezGene = 17687
    | Mm_Ensembl = ENSMUSG00000007035
    | Mm_RefseqmRNA = NM_013600
    | Mm_RefseqProtein = NP_038628
    | Mm_GenLoc_db = 
    | Mm_GenLoc_chr = 17
    | Mm_GenLoc_start = 34636661
    | Mm_GenLoc_end = 34654782
    | Mm_Uniprot = Q9R1I5
  }}
}}
'''MutS homolog 5 (E. coli)''', also known as '''MSH5''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: MSH5 mutS homolog 5 (E. coli)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4439| accessdate = }}</ref>


<!-- The PBB_Summary template is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair or meiotic recombination processes. This protein is similar to a Saccharomyces cerevisiae protein that participates in meiotic segregation fidelity and crossing-over. This protein forms heterooligomers with another member of this family, mutS homolog 4. Alternative splicing results in four transcript variants encoding three different isoforms.<ref name="entrez"/>
{{PBB_Summary
| section_title =
| summary_text = This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair or meiotic recombination processes. This protein is similar to a Saccharomyces cerevisiae protein that participates in meiotic segregation fidelity and crossing-over. This protein forms heterooligomers with another member of this family, mutS homolog 4. Alternative splicing results in four transcript variants encoding three different isoforms.<ref name="entrez">{{cite web | title = Entrez Gene: MSH5 mutS homolog 5 (E. coli)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4439| accessdate = }}</ref>
}}


==References==
== Mutations ==
{{reflist|2}}
 
==Further reading==
Mice [[Zygosity#homozygous|homozygous]] for a null Msh5 mutation (Msh5-/-) are viable but sterile.<ref name="pmid9916805">{{cite journal | vauthors = Edelmann W, Cohen PE, Kneitz B, Winand N, Lia M, Heyer J, Kolodner R, Pollard JW, Kucherlapati R | title = Mammalian MutS homologue 5 is required for chromosome pairing in meiosis | journal = Nature Genetics | volume = 21 | issue = 1 | pages = 123–7 | date = Jan 1999 | pmid = 9916805 | doi = 10.1038/5075 }}</ref> In these mice, the [[Meiosis#prophase I|prophase I]] stage of [[meiosis]] is defective due to the disruption of [[Bivalent (genetics)|chromosome pairing]]. This meiotic failure leads, in male mice, to diminution of [[testicle|testicular]] size, and in female mice, to a complete loss of [[Ovary|ovarian]] structures.
{{refbegin | 2}}
 
{{PBB_Further_reading
A genetic investigation was performed to test women with premature ovarian failure for mutations in each of four meiotic genes.<ref name="pmid18166824">{{cite journal | vauthors = Mandon-Pépin B, Touraine P, Kuttenn F, Derbois C, Rouxel A, Matsuda F, Nicolas A, Cotinot C, Fellous M | title = Genetic investigation of four meiotic genes in women with premature ovarian failure | journal = European Journal of Endocrinology / European Federation of Endocrine Societies | volume = 158 | issue = 1 | pages = 107–15 | date = Jan 2008 | pmid = 18166824 | doi = 10.1530/EJE-07-0400 }}</ref>  Among 41 women with premature ovarian failure two were found to be [[Zygosity#heterozygous|heterozygous]] for a mutation in the MSH5 gene; among 34 fertile women (controls) no mutations were found in the four tested genes.
| citations =  
 
*{{cite journal  | author=Her C, Zhao N, Wu X, Tompkins JD |title=MutS homologues hMSH4 and hMSH5: diverse functional implications in humans. |journal=Front. Biosci. |volume=12 |issue=  |pages= 905-11 |year= 2007 |pmid= 17127347 |doi= }}
These findings in mouse and human indicate that the MSH5 protein plays an important role in meiotic recombination.
*{{cite journal | author=Sargent CA, Dunham I, Campbell RD |title=Identification of multiple HTF-island associated genes in the human major histocompatibility complex class III region. |journal=EMBO J. |volume=8 |issue= 8 |pages= 2305-12 |year= 1989 |pmid= 2477242 |doi= }}
 
*{{cite journal  | author=Albertella MR, Jones H, Thomson W, ''et al.'' |title=Localization of eight additional genes in the human major histocompatibility complex, including the gene encoding the casein kinase II beta subunit (CSNK2B). |journal=Genomics |volume=36 |issue= 2 |pages= 240-51 |year= 1997 |pmid= 8812450 |doi= 10.1006/geno.1996.0459 }}
In the worm ''[[Caenorhabditis elegans]]'', the MSH5 protein is required during meiosis both for normal spontaneous and for gamma-irradiation induced crossover recombination and chiasma formation.<ref name=Kelly>{{cite journal | vauthors = Kelly KO, Dernburg AF, Stanfield GM, Villeneuve AM | title = Caenorhabditis elegans msh-5 is required for both normal and radiation-induced meiotic crossing over but not for completion of meiosis | journal = Genetics | volume = 156 | issue = 2 | pages = 617–30 | date = Oct 2000 | pmid = 11014811 | pmc = 1461284 | doi = }}</ref> Meiotic recombination is often initiated by double strand breaks. MSH5 mutants retain the competence to repair DNA double-strand breaks that are present during meiosis, but they accomplish this repair in a way that does not lead to crossovers between homologous chromosomes.<ref name=Kelly />  The known mechanism of non-crossover recombinational repair is called synthesis dependent strand annealing (see [[homologous recombination]]; see also Bernstein et al.<ref>Harris Bernstein, Carol Bernstein and Richard E. Michod (2011). Meiosis as an Evolutionary Adaptation for DNA Repair. DNA Repair, Dr. Inna Kruman (Ed). {{ISBN|978-953-307-697-3}}, InTech, Available from http://www.intechopen.com/books/dna-repair/meiosis-as-an-evolutionary-adaptation-for-dna-repair.</ref>).  MSH5 thus appears to be employed in directing the [[Homologous recombination|recombinational repair]] of some double-strand breaks towards the cross over option rather than the non-cross over option.
*{{cite journal | author=Her C, Doggett NA |title=Cloning, structural characterization, and chromosomal localization of the human orthologue of Saccharomyces cerevisiae MSH5 gene. |journal=Genomics |volume=52 |issue= 1 |pages= 50-61 |year= 1999 |pmid= 9740671 |doi= 10.1006/geno.1998.5374 }}
 
*{{cite journal  | author=Winand NJ, Panzer JA, Kolodner RD |title=Cloning and characterization of the human and Caenorhabditis elegans homologs of the Saccharomyces cerevisiae MSH5 gene. |journal=Genomics |volume=53 |issue= 1 |pages= 69-80 |year= 1998 |pmid= 9787078 |doi= 10.1006/geno.1998.5447 }}
== Interactions ==
*{{cite journal | author=Edelmann W, Cohen PE, Kneitz B, ''et al.'' |title=Mammalian MutS homologue 5 is required for chromosome pairing in meiosis. |journal=Nat. Genet. |volume=21 |issue= 1 |pages= 123-7 |year= 1999 |pmid= 9916805 |doi= 10.1038/5075 }}
 
*{{cite journal | author=Bocker T, Barusevicius A, Snowden T, ''et al.'' |title=hMSH5: a human MutS homologue that forms a novel heterodimer with hMSH4 and is expressed during spermatogenesis. |journal=Cancer Res. |volume=59 |issue= 4 |pages= 816-22 |year= 1999 |pmid= 10029069 |doi=  }}
MSH5 has been shown to [[Protein-protein interaction|interact]] with [[MSH4]].<ref name=pmid9787078 /><ref name=pmid12591739>{{cite journal | vauthors = Her C, Wu X, Griswold MD, Zhou F | title = Human MutS homologue MSH4 physically interacts with von Hippel-Lindau tumor suppressor-binding protein 1 | journal = Cancer Research | volume = 63 | issue = 4 | pages = 865–72 | date = Feb 2003 | pmid = 12591739 }}</ref><ref name=pmid10029069>{{cite journal | vauthors = Bocker T, Barusevicius A, Snowden T, Rasio D, Guerrette S, Robbins D, Schmidt C, Burczak J, Croce CM, Copeland T, Kovatich AJ, Fishel R | title = hMSH5: a human MutS homologue that forms a novel heterodimer with hMSH4 and is expressed during spermatogenesis | journal = Cancer Research | volume = 59 | issue = 4 | pages = 816–22 | date = Feb 1999 | pmid = 10029069 }}</ref>
*{{cite journal  | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899-903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 }}
{{clear}}
*{{cite journal | author=Mungall AJ, Palmer SA, Sims SK, ''et al.'' |title=The DNA sequence and analysis of human chromosome 6. |journal=Nature |volume=425 |issue= 6960 |pages= 805-11 |year= 2003 |pmid= 14574404 |doi= 10.1038/nature02055 }}
== References ==
*{{cite journal | author=Xie T, Rowen L, Aguado B, ''et al.'' |title=Analysis of the gene-dense major histocompatibility complex class III region and its comparison to mouse. |journal=Genome Res. |volume=13 |issue= 12 |pages= 2621-36 |year= 2004 |pmid= 14656967 |doi= 10.1101/gr.1736803 }}
{{reflist|33em}}
*{{cite journal | author=Ota T, Suzuki Y, Nishikawa T, ''et al.'' |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40-5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }}
 
*{{cite journal | author=Anderson NL, Polanski M, Pieper R, ''et al.'' |title=The human plasma proteome: a nonredundant list developed by combination of four separate sources. |journal=Mol. Cell Proteomics |volume=3 |issue= 4 |pages= 311-26 |year= 2004 |pmid= 14718574 |doi= 10.1074/mcp.M300127-MCP200 }}
== Further reading ==
*{{cite journal | author=Snowden T, Acharya S, Butz C, ''et al.'' |title=hMSH4-hMSH5 recognizes Holliday Junctions and forms a meiosis-specific sliding clamp that embraces homologous chromosomes. |journal=Mol. Cell |volume=15 |issue= 3 |pages= 437-51 |year= 2004 |pmid= 15304223 |doi= 10.1016/j.molcel.2004.06.040 }}
{{refbegin|33em}}
*{{cite journal | author=Gerhard DS, Wagner L, Feingold EA, ''et al.'' |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121-7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 }}
* {{cite journal | vauthors = Her C, Zhao N, Wu X, Tompkins JD | title = MutS homologues hMSH4 and hMSH5: diverse functional implications in humans | journal = Frontiers in Bioscience | volume = 12 | issue = | pages = 905–11 | year = 2007 | pmid = 17127347 | doi = 10.2741/2112 }}
*{{cite journal | author=Yi W, Wu X, Lee TH, ''et al.'' |title=Two variants of MutS homolog hMSH5: prevalence in humans and effects on protein interaction. |journal=Biochem. Biophys. Res. Commun. |volume=332 |issue= 2 |pages= 524-32 |year= 2005 |pmid= 15907804 |doi= 10.1016/j.bbrc.2005.04.154 }}
* {{cite journal | vauthors = Sargent CA, Dunham I, Campbell RD | title = Identification of multiple HTF-island associated genes in the human major histocompatibility complex class III region | journal = The EMBO Journal | volume = 8 | issue = 8 | pages = 2305–12 | date = Aug 1989 | pmid = 2477242 | pmc = 401163 | doi = }}
*{{cite journal | author=Lee TH, Yi W, Griswold MD, ''et al.'' |title=Formation of hMSH4-hMSH5 heterocomplex is a prerequisite for subsequent GPS2 recruitment. |journal=DNA Repair (Amst.) |volume=5 |issue= 1 |pages= 32-42 |year= 2006 |pmid= 16122992 |doi= 10.1016/j.dnarep.2005.07.004 }}
* {{cite journal | vauthors = Albertella MR, Jones H, Thomson W, Olavesen MG, Campbell RD | title = Localization of eight additional genes in the human major histocompatibility complex, including the gene encoding the casein kinase II beta subunit (CSNK2B) | journal = Genomics | volume = 36 | issue = 2 | pages = 240–51 | date = Sep 1996 | pmid = 8812450 | doi = 10.1006/geno.1996.0459 }}
*{{cite journal | author=Rual JF, Venkatesan K, Hao T, ''et al.'' |title=Towards a proteome-scale map of the human protein-protein interaction network. |journal=Nature |volume=437 |issue= 7062 |pages= 1173-8 |year= 2005 |pmid= 16189514 |doi= 10.1038/nature04209 }}
* {{cite journal | vauthors = Edelmann W, Cohen PE, Kneitz B, Winand N, Lia M, Heyer J, Kolodner R, Pollard JW, Kucherlapati R | title = Mammalian MutS homologue 5 is required for chromosome pairing in meiosis | journal = Nature Genetics | volume = 21 | issue = 1 | pages = 123–7 | date = Jan 1999 | pmid = 9916805 | doi = 10.1038/5075 }}
*{{cite journal | author=Sekine H, Ferreira RC, Pan-Hammarström Q, ''et al.'' |title=Role for Msh5 in the regulation of Ig class switch recombination. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=104 |issue= 17 |pages= 7193-8 |year= 2007 |pmid= 17409188 |doi= 10.1073/pnas.0700815104 }}
* {{cite journal | vauthors = Bocker T, Barusevicius A, Snowden T, Rasio D, Guerrette S, Robbins D, Schmidt C, Burczak J, Croce CM, Copeland T, Kovatich AJ, Fishel R | title = hMSH5: a human MutS homologue that forms a novel heterodimer with hMSH4 and is expressed during spermatogenesis | journal = Cancer Research | volume = 59 | issue = 4 | pages = 816–22 | date = Feb 1999 | pmid = 10029069 | doi = }}
*{{cite journal | author=Szafranski K, Schindler S, Taudien S, ''et al.'' |title=Violating the splicing rules: TG dinucleotides function as alternative 3' splice sites in U2-dependent introns. |journal= |volume=8 |issue= 8 |pages= R154 |year=  |pmid= 17672918 |doi= 10.1186/gb-2007-8-8-r154 }}
* {{cite journal | vauthors = Xie T, Rowen L, Aguado B, Ahearn ME, Madan A, Qin S, Campbell RD, Hood L | title = Analysis of the gene-dense major histocompatibility complex class III region and its comparison to mouse | journal = Genome Research | volume = 13 | issue = 12 | pages = 2621–36 | date = Dec 2003 | pmid = 14656967 | pmc = 403804 | doi = 10.1101/gr.1736803 }}
}}
* {{cite journal | vauthors = Anderson NL, Polanski M, Pieper R, Gatlin T, Tirumalai RS, Conrads TP, Veenstra TD, Adkins JN, Pounds JG, Fagan R, Lobley A | title = The human plasma proteome: a nonredundant list developed by combination of four separate sources | journal = Molecular & Cellular Proteomics | volume = 3 | issue = 4 | pages = 311–26 | date = Apr 2004 | pmid = 14718574 | doi = 10.1074/mcp.M300127-MCP200 }}
* {{cite journal | vauthors = Snowden T, Acharya S, Butz C, Berardini M, Fishel R | title = hMSH4-hMSH5 recognizes Holliday Junctions and forms a meiosis-specific sliding clamp that embraces homologous chromosomes | journal = Molecular Cell | volume = 15 | issue = 3 | pages = 437–51 | date = Aug 2004 | pmid = 15304223 | doi = 10.1016/j.molcel.2004.06.040 }}
* {{cite journal | vauthors = Yi W, Wu X, Lee TH, Doggett NA, Her C | title = Two variants of MutS homolog hMSH5: prevalence in humans and effects on protein interaction | journal = Biochemical and Biophysical Research Communications | volume = 332 | issue = 2 | pages = 524–32 | date = Jul 2005 | pmid = 15907804 | doi = 10.1016/j.bbrc.2005.04.154 }}
* {{cite journal | vauthors = Lee TH, Yi W, Griswold MD, Zhu F, Her C | title = Formation of hMSH4-hMSH5 heterocomplex is a prerequisite for subsequent GPS2 recruitment | journal = DNA Repair | volume = 5 | issue = 1 | pages = 32–42 | date = Jan 2006 | pmid = 16122992 | doi = 10.1016/j.dnarep.2005.07.004 }}
* {{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 = Oct 2005 | pmid = 16189514 | doi = 10.1038/nature04209 }}
* {{cite journal | vauthors = Sekine H, Ferreira RC, Pan-Hammarström Q, Graham RR, Ziemba B, de Vries SS, Liu J, Hippen K, Koeuth T, Ortmann W, Iwahori A, Elliott MK, Offer S, Skon C, Du L, Novitzke J, Lee AT, Zhao N, Tompkins JD, Altshuler D, Gregersen PK, Cunningham-Rundles C, Harris RS, Her C, Nelson DL, Hammarström L, Gilkeson GS, Behrens TW | title = Role for Msh5 in the regulation of Ig class switch recombination | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 104 | issue = 17 | pages = 7193–8 | date = Apr 2007 | pmid = 17409188 | pmc = 1855370 | doi = 10.1073/pnas.0700815104 }}
* {{cite journal | vauthors = Szafranski K, Schindler S, Taudien S, Hiller M, Huse K, Jahn N, Schreiber S, Backofen R, Platzer M | title = Violating the splicing rules: TG dinucleotides function as alternative 3' splice sites in U2-dependent introns | journal = Genome Biology | volume = 8 | issue = 8 | pages = R154 | year = 2007 | pmid = 17672918 | pmc = 2374985 | doi = 10.1186/gb-2007-8-8-r154 }}
{{refend}}
{{refend}}
{{protein-stub}}
{{WikiDoc Sources}}

Latest revision as of 06:56, 4 September 2017

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez

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Ensembl

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UniProt

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RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

MutS protein homolog 5 is a protein that in humans is encoded by the MSH5 gene.[1][2][3][4]

Function

This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair or meiotic recombination processes. This protein is similar to a Saccharomyces cerevisiae protein that participates in meiotic segregation fidelity and crossing-over. This protein forms heterooligomers with another member of this family, mutS homolog 4. Alternative splicing results in four transcript variants encoding three different isoforms.[4]

Mutations

Mice homozygous for a null Msh5 mutation (Msh5-/-) are viable but sterile.[5] In these mice, the prophase I stage of meiosis is defective due to the disruption of chromosome pairing. This meiotic failure leads, in male mice, to diminution of testicular size, and in female mice, to a complete loss of ovarian structures.

A genetic investigation was performed to test women with premature ovarian failure for mutations in each of four meiotic genes.[6] Among 41 women with premature ovarian failure two were found to be heterozygous for a mutation in the MSH5 gene; among 34 fertile women (controls) no mutations were found in the four tested genes.

These findings in mouse and human indicate that the MSH5 protein plays an important role in meiotic recombination.

In the worm Caenorhabditis elegans, the MSH5 protein is required during meiosis both for normal spontaneous and for gamma-irradiation induced crossover recombination and chiasma formation.[7] Meiotic recombination is often initiated by double strand breaks. MSH5 mutants retain the competence to repair DNA double-strand breaks that are present during meiosis, but they accomplish this repair in a way that does not lead to crossovers between homologous chromosomes.[7] The known mechanism of non-crossover recombinational repair is called synthesis dependent strand annealing (see homologous recombination; see also Bernstein et al.[8]). MSH5 thus appears to be employed in directing the recombinational repair of some double-strand breaks towards the cross over option rather than the non-cross over option.

Interactions

MSH5 has been shown to interact with MSH4.[2][9][10]

References

  1. ↑ Her C, Doggett NA (Aug 1998). "Cloning, structural characterization, and chromosomal localization of the human orthologue of Saccharomyces cerevisiae MSH5 gene". Genomics. 52 (1): 50–61. doi:10.1006/geno.1998.5374. PMID 9740671.
  2. ↑ 2.0 2.1 Winand NJ, Panzer JA, Kolodner RD (Oct 1998). "Cloning and characterization of the human and Caenorhabditis elegans homologs of the Saccharomyces cerevisiae MSH5 gene". Genomics. 53 (1): 69–80. doi:10.1006/geno.1998.5447. PMID 9787078.
  3. ↑ Snowden T, Shim KS, Schmutte C, Acharya S, Fishel R (Jan 2008). "hMSH4-hMSH5 adenosine nucleotide processing and interactions with homologous recombination machinery". The Journal of Biological Chemistry. 283 (1): 145–54. doi:10.1074/jbc.M704060200. PMC 2841433. PMID 17977839.
  4. ↑ 4.0 4.1 "Entrez Gene: MSH5 mutS homolog 5 (E. coli)".
  5. ↑ Edelmann W, Cohen PE, Kneitz B, Winand N, Lia M, Heyer J, Kolodner R, Pollard JW, Kucherlapati R (Jan 1999). "Mammalian MutS homologue 5 is required for chromosome pairing in meiosis". Nature Genetics. 21 (1): 123–7. doi:10.1038/5075. PMID 9916805.
  6. ↑ Mandon-Pépin B, Touraine P, Kuttenn F, Derbois C, Rouxel A, Matsuda F, Nicolas A, Cotinot C, Fellous M (Jan 2008). "Genetic investigation of four meiotic genes in women with premature ovarian failure". European Journal of Endocrinology / European Federation of Endocrine Societies. 158 (1): 107–15. doi:10.1530/EJE-07-0400. PMID 18166824.
  7. ↑ 7.0 7.1 Kelly KO, Dernburg AF, Stanfield GM, Villeneuve AM (Oct 2000). "Caenorhabditis elegans msh-5 is required for both normal and radiation-induced meiotic crossing over but not for completion of meiosis". Genetics. 156 (2): 617–30. PMC 1461284. PMID 11014811.
  8. ↑ Harris Bernstein, Carol Bernstein and Richard E. Michod (2011). Meiosis as an Evolutionary Adaptation for DNA Repair. DNA Repair, Dr. Inna Kruman (Ed). ISBN 978-953-307-697-3, InTech, Available from http://www.intechopen.com/books/dna-repair/meiosis-as-an-evolutionary-adaptation-for-dna-repair.
  9. ↑ Her C, Wu X, Griswold MD, Zhou F (Feb 2003). "Human MutS homologue MSH4 physically interacts with von Hippel-Lindau tumor suppressor-binding protein 1". Cancer Research. 63 (4): 865–72. PMID 12591739.
  10. ↑ Bocker T, Barusevicius A, Snowden T, Rasio D, Guerrette S, Robbins D, Schmidt C, Burczak J, Croce CM, Copeland T, Kovatich AJ, Fishel R (Feb 1999). "hMSH5: a human MutS homologue that forms a novel heterodimer with hMSH4 and is expressed during spermatogenesis". Cancer Research. 59 (4): 816–22. PMID 10029069.

Further reading

Retrieved from "https://www.wikidoc.org/index.php?title=MSH5&oldid=1421033"