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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
MeSH Review

Hepatophyta

 
 
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High impact information on Hepatophyta

  • Nucleotide sequences of chloroplast 5S ribosomal RNA from cell suspension cultures of the liverworts Marchantia polymorpha and Jungermannia subulata [1].
  • Taken together, the data (1) support a sister group relationship of liverworts as a whole to all other embryophytes, (2) indicate loss of a group I and serial entries of group II introns in the nad5 gene during early evolution of the nonliverwort lineage, and (3) propose a placement of hornworts as sister group to tracheophytes [2].
  • The seed plants and simple leafy liverworts each independently derived a low level of bias in rbcL, perhaps indicating relaxed selectional constraint on molecular changes in the gene [3].
  • We present the nad2 gene structures in hornworts and liverworts and in the presumptive earliest-branching vascular land plant clade, the Lycopodiopsida [4].
  • These intron distribution patterns are consistent with the hypothesis that liverworts represent the basal-most land plants and that the two introns were gained in the common ancestor of mosses-hornworts-vascular plants after liverworts had diverged [5].
 

Biological context of Hepatophyta

  • The necessity for RNA editing to reconstitute conserved codon entities in nad2 is obvious for all clades except the marchantiid liverworts [4].
  • A survey of mitochondrial plant genomes revealed intron-containing tRNA genes are rather rare features, with the exception of tRNASerGCU genes in liverworts and peat-mosses [6].
 

Anatomical context of Hepatophyta

 

Associations of Hepatophyta with chemical compounds

  • Involvement of the mevalonic acid pathway and the glyceraldehyde-pyruvate pathway in terpenoid biosynthesis of the liverworts Ricciocarpos natans and Conocephalum conicum [8].
  • Lunularic acid, a common growth inhibitor of liverworts, and five of its synthetic derivatives have also been tested, and two derivatives were found to be highly active [9].
  • A capillary zone electrophoresis (CZE) procedure for the determination of l-ascorbic acid (AA) and total ascorbic acid (TAA, as the sum of AA and dehydroascorbic acid) in vascular plants, lichens, bryophytes, and liverworts is described [10].
  • The incorporation of 13C-labeled glucose into borneol, bornyl acetate, the sesquiterpenes cubebanol and ricciocarpin A, phytol, and stigmasterol has been studied in axenic cultures of the liverworts Ricciocarpos natans and Conocephalum conicum [8].
  • Lignan derivatives from the liverwort Bazzania trilobata [11].

References

  1. Nucleotide sequences of chloroplast 5S ribosomal RNA from cell suspension cultures of the liverworts Marchantia polymorpha and Jungermannia subulata. Yamano, Y., Ohyama, K., Komano, T. Nucleic Acids Res. (1984) [Pubmed]
  2. Ancestors of trans-splicing mitochondrial introns support serial sister group relationships of hornworts and mosses with vascular plants. Groth-Malonek, M., Pruchner, D., Grewe, F., Knoop, V. Mol. Biol. Evol. (2005) [Pubmed]
  3. Evolutionary patterns of codon usage in the chloroplast gene rbcL. Wall, D.P., Herbeck, J.T. J. Mol. Evol. (2003) [Pubmed]
  4. Divergent intron conservation in the mitochondrial nad2 gene: signatures for the three bryophyte classes (mosses, liverworts, and hornworts) and the lycophytes. Pruchner, D., Beckert, S., Muhle, H., Knoop, V. J. Mol. Evol. (2002) [Pubmed]
  5. Distribution of introns in the mitochondrial gene nad1 in land plants: phylogenetic and molecular evolutionary implications. Dombrovska, O., Qiu, Y.L. Mol. Phylogenet. Evol. (2004) [Pubmed]
  6. New DNA markers for discrimination between closely-related species and for the reconstruction of historical events; an example using liverworts. Szweykowska-Kulińska, Z., Pacak, A., Jankowiak, K. Cell. Mol. Biol. Lett. (2002) [Pubmed]
  7. Bis(bibenzyls) from liverworts inhibit lipopolysaccharide-induced inducible NOS in RAW 264.7 cells: a study of structure-activity relationships and molecular mechanism. Harinantenaina, L., Quang, D.N., Takeshi, N., Hashimoto, T., Kohchi, C., Soma, G., Asakawa, Y. J. Nat. Prod. (2005) [Pubmed]
  8. Involvement of the mevalonic acid pathway and the glyceraldehyde-pyruvate pathway in terpenoid biosynthesis of the liverworts Ricciocarpos natans and Conocephalum conicum. Adam, K.P., Thiel, R., Zapp, J., Becker, H. Arch. Biochem. Biophys. (1998) [Pubmed]
  9. Molluscicidal properties of constituents from the liverwort Ricciocarpos natans and of synthetic lunularic acid derivatives. Wurzel, G., Becker, H., Eicher, T., Tiefensee, K. Planta Med. (1990) [Pubmed]
  10. Determination of L-ascorbic acid and total ascorbic acid in vascular and nonvascular plants by capillary zone electrophoresis. Herrero-Martínez, J.M., Simó-Alfonso, E., Deltoro, V.I., Calatayud, A., Ramis-Ramos, G. Anal. Biochem. (1998) [Pubmed]
  11. Lignan derivatives from the liverwort Bazzania trilobata. Scher, J.M., Zapp, J., Becker, H. Phytochemistry (2003) [Pubmed]
 
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