Physcomitrella patens explained

Physcomitrella patens is a synonym of Physcomitrium patens,[1] [2] the spreading earthmoss.[3] It is a moss, a bryophyte used as a model organism for studies on plant evolution, development, and physiology.[2]

Distribution and ecology

Physcomitrella patens is an early colonist of exposed mud and earth around the edges of pools of water.[4] P. patens has a disjunct distribution in temperate parts of the world, with the exception of South America.[5] The standard laboratory strain is the "Gransden" isolate, collected by H. Whitehouse from Gransden Wood, in Cambridgeshire in 1962.[6]

Model organism

See also: Knockout moss.

Mosses share fundamental genetic and physiological processes with vascular plants, although the two lineages diverged early in land-plant evolution.[7] A comparative study between modern representatives of the two lines may give insight into the evolution of mechanisms that contribute to the complexity of modern plants. In this context, P. patens is used as a model organism.[7] [2]

P. patens is one of a few known multicellular organisms with highly efficient homologous recombination.[8] [9] meaning that an exogenous DNA sequence can be targeted to a specific genomic position (a technique called gene targeting) to create knockout mosses. This approach is called reverse genetics and it is a powerful and sensitive tool to study the function of genes and, when combined with studies in higher plants such as Arabidopsis thaliana, can be used to study molecular plant evolution.

The targeted deletion or alteration of moss genes relies on the integration of a short DNA strand at a defined position in the genome of the host cell. Both ends of this DNA strand are engineered to be identical to this specific gene locus. The DNA construct is then incubated with moss protoplasts in the presence of polyethylene glycol. As mosses are haploid organisms, the regenerating moss filaments (protonemata) can be directly assayed for gene targeting within 6 weeks using PCR methods.[10] The first study using knockout moss appeared in 1998 and functionally identified ftsZ as a pivotal gene for the division of an organelle in a eukaryote.[11]

In addition, P. patens is increasingly used in biotechnology. Examples are the identification of moss genes with implications for crop improvement or human health[12] and the safe production of complex biopharmaceuticals in moss bioreactors.[13] By multiple gene knockout Physcomitrella plants were engineered that lack plant-specific post-translational protein glycosylation. These knockout mosses are used to produce complex biopharmaceuticals in a process called molecular farming.[14]

The genome of P. patens, with about 500 megabase pairs organized into 27 chromosomes, was completely sequenced in 2008.[7] [15]

Physcomitrella ecotypes, mutants, and transgenics are stored and made freely available to the scientific community by the International Moss Stock Center (IMSC). The accession numbers given by the IMSC can be used for publications to ensure safe deposit of newly described moss materials.

Lifecycle

Like all mosses, the lifecycle of P. patens is characterized by an alternation of two generations: a haploid gametophyte that produces gametes and a diploid sporophyte where haploid spores are produced.[16]

A spore develops into a filamentous structure called protonema, composed of two types of cells – chloronema with large and numerous chloroplasts and caulonema with very fast growth. Protonema filaments grow exclusively by tip growth of their apical cells and can originate side branches from subapical cells. Some side-branch initial cells can differentiate into buds rather than side branches. These buds give rise to gametophores (0.5–5.0 mm[17]), more complex structures bearing leaf-like structures, rhizoids, and the sexual organs: female archegonia and male antheridia. P. patens is monoicous, meaning that male and female organs are produced in the same plant. If water is available, flagellate sperm cells can swim from the antheridia to an archegonium and fertilize the egg within. The resulting diploid zygote develops into a sporophyte composed of a foot, seta, and capsule, where thousands of haploid spores are produced by meiosis.[18]

DNA repair and homologous recombination

P. patens is an excellent model in which to analyze repair of DNA damages in plants by the homologous recombination pathway. Failure to repair double-strand breaks and other DNA damages in somatic cells by homologous recombination can lead to cell dysfunction or death, and when failure occurs during meiosis, it can cause loss of gametes. The genome sequence of P. patens has revealed the presence of numerous genes that encode proteins necessary for repair of DNA damages by homologous recombination and by other pathways. PpRAD51, a protein at the core of the homologous recombination repair reaction, is required to preserve genome integrity in P. patens.[19] Loss of PpRAD51 causes marked hypersensitivity to the double-strand break-inducing agent bleomycin, indicating that homologous recombination is used for repair of somatic cell DNA damages. PpRAD51 is also essential for resistance to ionizing radiation.[20]

The DNA mismatch repair protein PpMSH2 is a central component of the P. patens mismatch repair pathway that targets base pair mismatches arising during homologous recombination. The PpMsh2 gene is necessary in P. patens to preserve genome integrity.[21] Genes Ppmre11 and Pprad50 of P. patens encode components of the MRN complex, the principal sensor of DNA double-strand breaks.[22] These genes are necessary for accurate homologous recombinational repair of DNA damages in P. patens. Mutant plants defective in either Ppmre11 or Pprad50 exhibit severely restricted growth and development (possibly reflecting accelerated senescence), and enhanced sensitivity to UV-B and bleomycin-induced DNA damage compared to wild-type plants.

Taxonomy

P. patens was first described by Johann Hedwig in his 1801 work Latin: Species Muscorum Frondosorum, under the name Phascum patens.[23] Physcomitrella is sometimes treated as a synonym of the genus Aphanorrhegma, in which case P. patens is known as Aphanorrhegma patens.[24] The generic name Physcomitrella implies a resemblance to Physcomitrium, which is named for its large calyptra, unlike that of Physcomitrella.[17] In 2019 it was proposed that the correct name for this moss is Physcomitrium patens.[2]

References

Further reading

External links

Notes and References

  1. Medina. Rafael. Johnson. Matthew G.. Liu. Yang. Wickett. Norman J.. Shaw. A. Jonathan. Goffinet. Bernard. 2019. Phylogenomic delineation of Physcomitrium (Bryophyta: Funariaceae) based on targeted sequencing of nuclear exons and their flanking regions rejects the retention of Physcomitrella, Physcomitridium and Aphanorrhegma. Journal of Systematics and Evolution. en. 57. 4. 404–417. 10.1111/jse.12516. 1759-6831. free.
  2. The Moss Physcomitrium (Physcomitrella) patens: A Model Organism for Non-Seed Plants . Stefan A . Rensing . Bernard . Goffinet . Rabea . Meyberg . Shu-Zon . Wu . Magdalena . Bezanilla . The Plant Cell . 32 . 5 . 2020 . 1361–1376 . 10.1105/tpc.19.00828 . 7203925 .
  3. Book: Edwards, Sean R.. 2012. English Names for British Bryophytes. Wootton, Northampton. British Bryological Society. 978-0-9561310-2-7. 0268-8034. British Bryological Society Special Volume. 5. 4.
  4. Book: Nick Hodgetts . 2010 . Aphanorrhegma patens (Physcomitrella patens), spreading earth-moss . 567 . Mosses and Liverworts of Britain and Ireland: a Field Guide . Ian Atherton . Sam Bosanquet . Mark Lawley . . 978-0-9561310-1-0 . http://www.bbsfieldguide.org.uk/sites/default/files/pdfs/mosses/Aphanorrhegma_patens.pdf .
  5. Book: Stefan A. Rensing, Daniel Lang & Andreas D. Zimmer . The Moss Physcomitrella patens . 2009 . Comparative genomics . 42–75 . https://books.google.com/books?id=IEzoQAH1EdEC&pg=PA42 . 10.1111/b.9781405181891.2009.00003.x. 9781444316070 . In: Knight et al. (2009).
  6. Andrew Cuming . 2011 . Molecular bryology: mosses in the genomic era . Field Bryology . 103 . 9–13 .
  7. Stefan A. Rensing . Daniel Lang . Andreas D. Zimmer . Astrid Terry . Asaf Salamov . Harris Shapiro . Tomoaki Nishiyama . Pierre-François Perroud . Erika A. Lindquist . Yasuko Kamisugi . Takako Tanahashi . Keiko Sakakibara . Tomomichi Fujita . Kazuko Oishi . Tadasu Shin-I . Yoko Kuroki . Atsushi Toyoda . Yutaka Suzuki . Shin-ichi Hashimoto . Kazuo Yamaguchi . Sumio Sugano . Yuji Kohara . Asao Fujiyama . Aldwin Anterola . Setsuyuki Aoki . Neil Ashton . W. Brad Barbazuk . Elizabeth Barker . Jeffrey L. Bennetzen . Robert Blankenship . Sung Hyun Cho . Susan K. Dutcher . Mark Estelle . Jeffrey A. Fawcett . Heidrun Gundlach . Kousuke Hanada . Alexander Heyl . Karen A. Hicks . Jon Hughes . Martin Lohr . Klaus Mayer . Alexander Melkozernov . Takashi Murata . David R. Nelson . Birgit Pils . Michael Prigge . Bernd Reiss . Tanya Renner . Stephane Rombauts . Paul J. Rushton . Anton Sanderfoot . Gabriele Schween . Shin-Han Shiu . Kurt Stueber . Frederica L. Theodoulou . Hank Tu . Yves Van de Peer . Paul J. Verrier . Elizabeth Waters . Andrew Wood . Lixing Yang . David Cove . Andrew C. Cuming . Mitsuyasu Hasebe . Susan Lucas . Brent D. Mishler . Ralf Reski . Igor V. Grigoriev . Ralph S. Quatrano . Jeffrey L. Boore . 2008 . The Physcomitrella genome reveals evolutionary insights into the conquest of land by plants . . 319 . 5859 . 64–69 . 18079367 . 2008Sci...319...64R . 10.1126/science.1150646. 11858/00-001M-0000-0012-3787-A . 11115152 . free .
  8. Didier G. Schaefer . Jean-Pierre Zrÿd . amp . 1997 . Efficient gene targeting in the moss Physcomitrella patens . . 11 . 6 . 1195–1206 . 9225463 . 10.1046/j.1365-313X.1997.11061195.x.
  9. Didier G. Schaefer . 2002 . A new moss genetics: targeted mutagenesis in Physcomitrella patens . . 53 . 477–501 . 12221986 . 10.1146/annurev.arplant.53.100301.135202.
  10. Annette Hohe . Tanja Egener . JanM. Lucht . Hauke Holtorf . Christina Reinhard . Gabriele Schween . Ralf Reski . An improved and highly standardised transformation procedure allows efficient production of single and multiple targeted gene-knockouts in a moss, Physcomitrella patens . . 44 . 6 . 339–347 . 2004 . 14586556 . 10.1007/s00294-003-0458-4. 45780217 .
  11. René Strepp . Sirkka Scholz . Sven Kruse . Volker Speth . Ralf Reski . Plant nuclear gene knockout reveals a role in plastid division for the homolog of the bacterial cell division protein ftsZ, an ancestral tubulin . . 95 . 8 . 4368–4373 . 1998 . 9539743 . 22495 . 10.1073/pnas.95.8.4368 . 44902. 1998PNAS...95.4368S . free .
  12. Ralf Reski & Wolfgang Frank . 2005 . Moss (Physcomitrella patens) functional genomics – gene discovery and tool development with implications for crop plants and human health . . 4 . 48–57 . 15975264 . 10.1093/bfgp/4.1.48 . 1 . free .
  13. . 2007 . Moss bioreactors producing improved biopharmaceuticals . . 18 . 5 . 393–398 . 10.1016/j.copbio.2007.07.012 . 17869503.
  14. Anna Koprivova . Christian Stemmer . Friedrich Altmann . Axel Hoffmann . Stanislav Kopriva . Gilbert Gorr . Ralf Reski . Eva L. Decker . 2004 . Targeted knockouts of Physcomitrella lacking plant-specific immunogenic N-glycans . . 2 . 6 . 517–523 . 17147624 . 10.1111/j.1467-7652.2004.00100.x.
  15. Ralf Reski, Merle Faust, Xiao-Hui Wang, Michael Wehe & Wolfgang O. Abel . 1994 . Genome analysis of the moss Physcomitrella patens (Hedw.) B.S.G. . . 244 . 4 . 352–359 . 10.1007/BF00286686 . 8078460. 36669399 .
  16. 33 . 22 . 1175-1181 . 2023 . Mosses . Volker M . Lueth . Ralf . Reski . Current Biology . 10.1016/j.cub.2023.09.042 .
  17. Web site: Bernard Goffinet . 2005 . Physcomitrella . Bryophyte Flora of North America, Provisional Publication . . October 28, 2012.
  18. Jessica M . Budke . Ernest C . Bernard . Dennis J . Gray . Sanna . Huttunen . Birgit . Piechulla . Robert N . Trigiano . 2018 . Introduction to the special issue on bryophytes . Critical Reviews in Plant Sciences . 37 . 2-3 . 102-112 . 10.1080/07352689.2018.1482396 .
  19. Markmann-Mulisch U, Wendeler E, Zobell O, Schween G, Steinbiss HH, Reiss B . Differential requirements for RAD51 in Physcomitrella patens and Arabidopsis thaliana development and DNA damage repair . Plant Cell . 19 . 10 . 3080–9 . October 2007 . 17921313 . 2174717 . 10.1105/tpc.107.054049 .
  20. Schaefer DG, Delacote F, Charlot F, Vrielynck N, Guyon-Debast A, Le Guin S, Neuhaus JM, Doutriaux MP, Nogué F . RAD51 loss of function abolishes gene targeting and de-represses illegitimate integration in the moss Physcomitrella patens . DNA Repair (Amst.) . 9 . 5 . 526–33 . May 2010 . 20189889 . 10.1016/j.dnarep.2010.02.001 .
  21. Trouiller B, Schaefer DG, Charlot F, Nogué F . MSH2 is essential for the preservation of genome integrity and prevents homeologous recombination in the moss Physcomitrella patens . Nucleic Acids Res. . 34 . 1 . 232–42 . 2006 . 16397301 . 1325206 . 10.1093/nar/gkj423 .
  22. Kamisugi Y, Schaefer DG, Kozak J, Charlot F, Vrielynck N, Holá M, Angelis KJ, Cuming AC, Nogué F . MRE11 and RAD50, but not NBS1, are essential for gene targeting in the moss Physcomitrella patens . Nucleic Acids Res. . 40 . 8 . 3496–510 . April 2012 . 22210882 . 3333855 . 10.1093/nar/gkr1272 .
  23. Web site: !Physcomitrella patens (Hedw.) Bruch & Schimp. . . . October 28, 2012.
  24. Book: Celia Knight, Pierre-François Perroud . David Cove . amp . 2009 . Preface . xiii–xiv . https://books.google.com/books?id=IEzoQAH1EdEC&pg=PR13 . 10.1002/9781444316070.fmatter. Front Matter . 9781444316070 . In: Knight et al. (2009).

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