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DMC1 (gene)

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For the video game, see Devil May Cry (video game).

Meiotic recombination protein DMC1/LIM15 homolog is a protein that in humans is encoded by the DMC1 gene.[5][6][7][8]

DMC1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesDMC1, DMC1H, LIM15, dJ199H16.1, DNA meiotic recombinase 1
External IDsOMIM: 602721; MGI: 105393; HomoloGene: 5135; GeneCards: DMC1; OMA:DMC1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

11144

13404

Ensembl

ENSG00000100206

ENSMUSG00000022429

UniProt

Q14565

Q61880

RefSeq (mRNA)

NM_001278208
NM_007068
NM_001363017

NM_001278226
NM_010059

RefSeq (protein)

NP_001265137
NP_008999
NP_001349946

NP_001265155
NP_034189

Location (UCSC)Chr 22: 38.52 – 38.57 MbChr 15: 79.45 – 79.49 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Meiotic recombination protein Dmc1 is a homolog of the bacterial strand exchange protein RecA. Dmc1 plays the central role in homologous recombination in meiosis by assembling at the sites of programmed DNA double strand breaks and carrying out a search for allelic DNA sequences located on homologous chromatids. The name "Dmc" stands for "disrupted meiotic cDNA" and refers to the method used for its discovery which involved using clones from a meiosis-specific cDNA library to direct knock-out mutations of abundantly expressed meiotic genes

The Dmc1 protein is one of two homologs of RecA found in eukaryotic cells, the other being Rad51. DMC1 and RAD51 share over 50% amino acid similarity.[9] In budding yeast, Rad51 serves as a strand exchange protein in mitosis where it is critical for the repair of DNA breaks. Rad51 is converted to an accessory factor for Dmc1 during meiosis by inhibition of its strand exchange activity.[10] Homologs of DMC1 are well conserved and have been identified in many organisms including divergent fungi, plants and mammals including humans.[5][6][7][8]

Discovery

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The DMC1 gene and protein were discovered in the budding yeast S. cerevisiae by Douglas Bishop in 1992 when he was a postdoctoral fellow in the laboratory of Nancy Kleckner at Harvard University.[11]

Structure

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Human DMC1 is a homomultimer in the form of an octameric ring with a diameter of 140 Å and a hole in the middle of 45 Å.[12][9] DMC1 binds preferentially to ssDNA over dsDNA.[12] Unlike RecA and Rad51, DMC1 does not appear to form a helical filament on DNA, instead forming rings with DNA passing through the center.[12] hDMC1 can conduct D-loop formation in supercoiled DNA.[13] DMC1 has weak ATPase activity and is able to promote heteroduplex formation in the presence of a non-hydrolysable analog of ATP, indicating a requirement for ATP binding over ATP hydrolysis.[14] DMC1 also shows enhanced binding to nucleosomes with histone tails removed, indicating that chromosome architecture may play a role in DMC1 binding, but not Rad51.[15]

Function

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The protein encoded by this gene is essential for meiotic homologous recombination. Genetic recombination in meiosis plays an important role in generating diversity of genetic information and facilitates the reductional segregation of chromosomes that must occur for formation of gametes during sexual reproduction.

During meiosis, programmed DNA double strand breaks (DSBs) are introduced by topoisomerase-like enzyme Spo11. DSBs are lengthened through the actions of exonucleases to trim the 5' ends and form long 3' single-stranded DNA (ssDNA) overhangs. These 3' overhangs are stabilized by the effects of single strand binding proteins (SSBs) to protect the ssDNA and prevent the formation of secondary structures. DMC1 is loaded onto the 3' ssDNA to form a right-handed helical nucleoprotein filament. Subsequently, this nucleoprotein filament conducts a homology search in a homologous DNA region. Single-strand invasion in a complementary region in the homologous chromosome by the 3'-ended DNA strand forms a heteroduplex in the form of a displacement loop (D-loop). This D-Loop is extended as DNA repair synthesis occurs, forming a Holliday junction. Resolution of this Holiday junction results in crossover or non-crossover product.[16] Crossover products are generated to a lesser extent than non-crossover products.[17]

Like other members of the Rad51/RecA family, Dmc1 stabilizes strand exchange intermediates (Rad1/RecA-stretched DNA, or RS-DNA) in stretched triplets similar to B form DNA. Each molecule of the protein binds a triplet of nucleotides, and the strength of that binding, as assessed by the change in Gibbs free energy, can be assessed by the length of time that a labelled dsDNA probe with a short homologous sequence remains bound to a DNA containing a short region of homology to it. A study of this type has shown that a mismatch in any of the three positions at the end of a stretch of homology will not increase the length of time that the probe remains bound, and in Rad51 or RecA constructs an internal mismatch will cause a similar reduction in binding time. All of the enzymes are capable of "stepping over" a mismatch and continuing to bind the probe more firmly if a longer region of homology exists. However, with Dmc1 a triplet with a single internal (but not terminal) mismatch will contribute to the stability of probe binding to a similar extent as one without a mismatch. In this way, Dmc1 is specially suited to its role as a meiosis-specific recombinase, as this activity permits it more effectively to catalyze recombination between sequences that are not perfectly matched.[18]

Interactions

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DMC1 (gene) has been shown to interact with RAD51 and the Structural Maintenance of Chromosome 5/6 (SMC5/6) complex.[19][14] The protein has also been shown to bind Tid1(Rdh54), Mei5/Sae3, and Hop2/Mnd1. All of these interacting proteins act to enhance Dmc1's activity in purified systems and are also implicated as being required for Dmc1 function in cells.

DMC1 has also been shown to interact with FIGNL1. FIGNL1 is believed to promote the disassembly of DMC1 during male meiosis.[20]

Rad51

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During meiosis, the two recombinases, Rad51 and Dmc1, interact with single-stranded DNA to form specialized filaments that are adapted for facilitating recombination between homologous chromosomes. Both Dmc1 and Rad51 have an intrinsic ability to self-aggregate.[21] The presence of Rad51 filaments stabilizes adjacent Dmc1 filaments and conversely Dmc1 stabilizes adjacent Rad51 filaments. A model was proposed in which Dmc1 and Rad51 form separate filaments on the same single stranded DNA and cross-talk between the two recombinases affects their biochemical properties.[21]

During meiosis, even in the absence of Rad51 strand exchange activity, Dmc1 appears to be able to repair all meiotic DNA breaks, and this absence does not affect meiotic crossing over rates.[22]

Hop2/Mnd1

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Hop2 and Mnd1 associate into a heterodimer which itself has affinity for dsDNA, and to a lesser extent, ssDNA. Hop2/Mnd1 stimulates strand-exchange activity of DMC1 in vitro. The interaction of Hop2/Mnd1 and DMC1 are thought to promote preferential binding of DMC1 to ssDNA and bring homologs into close proximity.[23][24]

SCM5/6

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DMC1 interacts with the Structural Maintenance of Chromosomes 5/6 (SMC5/6) complex. SCM5/6 complex inhibits the formation of DNA intermediates and is involved in their resolution. There is evidence that SCM5/6 interacts with and inhibit meiotic localization of DMC1. Rad51 can inhibit this interaction, and this may be its role as an accessory factor during meiotic homologous recombination.[19]

Clinical significance

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Mutations in the DMC1 gene are associated with male infertility, due to nonobstructive azoospermia, where the testes produce little to no sperm.[25] In mice, a single amino acid change can prevent crossing over and lead to meiotic arrest through an autosomal dominant mechanism.[26]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000100206 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000022429 – 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. ^ a b Habu T, Taki T, West A, Nishimune Y, Morita T (February 1996). "The mouse and human homologs of DMC1, the yeast meiosis-specific homologous recombination gene, have a common unique form of exon-skipped transcript in meiosis". Nucleic Acids Research. 24 (3): 470–477. doi:10.1093/nar/24.3.470. PMC 145652. PMID 8602360.
  6. ^ a b Sato S, Seki N, Hotta Y, Tabata S (August 1995). "Expression profiles of a human gene identified as a structural homologue of meiosis-specific recA-like genes". DNA Research. 2 (4): 183–186. doi:10.1093/dnares/2.4.183. PMID 8590282.
  7. ^ a b Thorslund T, Esashi F, West SC (June 2007). "Interactions between human BRCA2 protein and the meiosis-specific recombinase DMC1". The EMBO Journal. 26 (12): 2915–2922. doi:10.1038/sj.emboj.7601739. PMC 1894777. PMID 17541404.
  8. ^ a b "Entrez Gene: DMC1 DMC1 dosage suppressor of mck1 homolog, meiosis-specific homologous recombination (yeast)".
  9. ^ a b Passy SI, Yu X, Li Z, Radding CM, Masson JY, West SC, Egelman EH (September 1999). "Human Dmc1 protein binds DNA as an octameric ring". Proceedings of the National Academy of Sciences of the United States of America. 96 (19): 10684–10688. Bibcode:1999PNAS...9610684P. doi:10.1073/pnas.96.19.10684. PMC 17943. PMID 10485886.
  10. ^ Cloud V, Chan YL, Grubb J, Budke B, Bishop DK (September 2012). "Rad51 is an accessory factor for Dmc1-mediated joint molecule formation during meiosis". Science. 337 (6099): 1222–1225. Bibcode:2012Sci...337.1222C. doi:10.1126/science.1219379. PMC 4056682. PMID 22955832.
  11. ^ Bishop DK, Park D, Xu L, Kleckner N (May 1992). "DMC1: a meiosis-specific yeast homolog of E. coli recA required for recombination, synaptonemal complex formation, and cell cycle progression". Cell. 69 (3): 439–456. doi:10.1016/0092-8674(92)90446-j. PMID 1581960. S2CID 45890186.
  12. ^ a b c Masson JY, West SC (February 2001). "The Rad51 and Dmc1 recombinases: a non-identical twin relationship". Trends in Biochemical Sciences. 26 (2): 131–136. doi:10.1016/S0968-0004(00)01742-4. PMID 11166572.
  13. ^ Li Z, Golub EI, Gupta R, Radding CM (October 1997). "Recombination activities of HsDmc1 protein, the meiotic human homolog of RecA protein". Proceedings of the National Academy of Sciences of the United States of America. 94 (21): 11221–11226. Bibcode:1997PNAS...9411221L. doi:10.1073/pnas.94.21.11221. PMC 23422. PMID 9326590.
  14. ^ a b Masson JY, Davies AA, Hajibagheri N, Van Dyck E, Benson FE, Stasiak AZ, et al. (November 1999). "The meiosis-specific recombinase hDmc1 forms ring structures and interacts with hRad51". The EMBO Journal. 18 (22): 6552–6560. doi:10.1093/emboj/18.22.6552. PMC 1171718. PMID 10562567.
  15. ^ Kobayashi W, Takaku M, Machida S, Tachiwana H, Maehara K, Ohkawa Y, Kurumizaka H (April 2016). "Chromatin architecture may dictate the target site for DMC1, but not for RAD51, during homologous pairing". Scientific Reports. 6: 24228. Bibcode:2016NatSR...624228K. doi:10.1038/srep24228. PMC 4823753. PMID 27052786.
  16. ^ Da Ines O, Bazile J, Gallego ME, White CI (August 2022). "DMC1 attenuates RAD51-mediated recombination in Arabidopsis". PLOS Genetics. 18 (8): e1010322. doi:10.1371/journal.pgen.1010322. PMC 9451096. PMID 36007010.
  17. ^ Hunter N (October 2015). "Meiotic Recombination: The Essence of Heredity". Cold Spring Harbor Perspectives in Biology. 7 (12): a016618. doi:10.1101/cshperspect.a016618. PMC 4665078. PMID 26511629.
  18. ^ Lee JY, Terakawa T, Qi Z, Steinfeld JB, Redding S, Kwon Y, et al. (August 2015). "DNA RECOMBINATION. Base triplet stepping by the Rad51/RecA family of recombinases". Science. 349 (6251): 977–981. doi:10.1126/science.aab2666. PMC 4580133. PMID 26315438.
  19. ^ a b Chen H, He C, Wang C, Wang X, Ruan F, Yan J, et al. (August 2021). "RAD51 supports DMC1 by inhibiting the SMC5/6 complex during meiosis". The Plant Cell. 33 (8): 2869–2882. doi:10.1093/plcell/koab136. PMC 8408460. PMID 34009315.
  20. ^ Ito M, Furukohri A, Matsuzaki K, Fujita Y, Toyoda A, Shinohara A (October 2023). "FIGNL1 AAA+ ATPase remodels RAD51 and DMC1 filaments in pre-meiotic DNA replication and meiotic recombination". Nature Communications. 14 (1): 6857. Bibcode:2023NatCo..14.6857I. doi:10.1038/s41467-023-42576-w. PMC 10611733. PMID 37891173.
  21. ^ a b Crickard JB, Kaniecki K, Kwon Y, Sung P, Greene EC (March 2018). "Spontaneous self-segregation of Rad51 and Dmc1 DNA recombinases within mixed recombinase filaments". The Journal of Biological Chemistry. 293 (11): 4191–4200. doi:10.1074/jbc.RA117.001143. PMC 5858004. PMID 29382724.
  22. ^ Singh G, Da Ines O, Gallego ME, White CI (2017). "Analysis of the impact of the absence of RAD51 strand exchange activity in Arabidopsis meiosis". PLOS ONE. 12 (8): e0183006. Bibcode:2017PLoSO..1283006S. doi:10.1371/journal.pone.0183006. PMC 5552350. PMID 28797117.
  23. ^ Bugreev DV, Huang F, Mazina OM, Pezza RJ, Voloshin ON, Camerini-Otero RD, Mazin AV (June 2014). "HOP2-MND1 modulates RAD51 binding to nucleotides and DNA". Nature Communications. 5 (1): 4198. Bibcode:2014NatCo...5.4198B. doi:10.1038/ncomms5198. PMC 4279451. PMID 24943459.
  24. ^ Chen YK, Leng CH, Olivares H, Lee MH, Chang YC, Kung WM, et al. (July 2004). "Heterodimeric complexes of Hop2 and Mnd1 function with Dmc1 to promote meiotic homolog juxtaposition and strand assimilation". Proceedings of the National Academy of Sciences of the United States of America. 101 (29): 10572–10577. Bibcode:2004PNAS..10110572C. doi:10.1073/pnas.0404195101. PMC 490024. PMID 15249670.
  25. ^ "DMC1 DNA meiotic recombinase 1 [Homo sapiens (human)] - Gene". National Center for Biotechnology Information (NCBI). U.S. National Library of Medicine. Retrieved 2023-12-05.
  26. ^ Bannister LA, Pezza RJ, Donaldson JR, de Rooij DG, Schimenti KJ, Camerini-Otero RD, Schimenti JC (May 2007). "A dominant, recombination-defective allele of Dmc1 causing male-specific sterility". PLOS Biology. 5 (5): e105. doi:10.1371/journal.pbio.0050105. PMC 1847842. PMID 17425408.

Further reading

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