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

Pecten

 
 
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Disease relevance of Pecten

  • At optic cup stages, however, noggin overexpression caused colobomas, pecten agenesis, replacement of the ventral RPE by neuroepithelium-like tissue, and ectopic expression of optic stalk markers in the region of the ventral retina and RPE [1].
  • Using these Pecten sequences, we have overexpressed the regulatory light chain, and a combination of essential light chain and myosin heavy chain fragment, separately, in E. coli BL21 (DE3) prior to recombination, thereby producing Pecten regulatory domains without recourse to proteolytic digestion [2].
 

High impact information on Pecten

  • Myosin from the striated adductor muscle of the scallop Pecten maximus is shown to fold into a compact 10 S conformer under relaxing conditions, as has been characterized for smooth and non-muscle myosins [3].
  • B-cadherin was located in the glia limitans perivascularis et superficialis of the pecten oculi and in a subset of cells at the retinal border [4].
  • By using these proteins from the scallop, Pecten maximus, the existence of two distinct tryptophan-containing domains was established, which respond independently to ATP and Ca2+-specific binding [5].
  • Octopine dehydrogenase from Pecten maximus: steady-state mechanism [6].
  • Using polymerase chain reaction-based approaches, we isolated 13 different Pecten maximus (Bivalvia: Pteriomorphia) sequences corresponding to all the genes of the four Hox cluster classes and to genes Xlox and Cdx of the ParaHox cluster [7].
 

Biological context of Pecten

 

Anatomical context of Pecten

  • Whereas perineural and choroid vessels remained immunonegative for N-cadherin, vascular sprouts invading both the brain and the pecten primordium acquired anti-N-cadherin immunoreactivity [9].
  • A single electrode voltage clamp was used to examine the prolonged hyperpolarizing afterpotential (PHA) which accompanies photoconversion of a substantial fraction of rhodopsin (lambda max = 500 nM) to metarhodopsin (lambda max = 575 nM) in distal photoreceptor cells in the retina of the bay scallop, Pecten irradians [10].
  • The use of sequential measurements of hemolymph cholinesterase activities as a non-invasive biomarker of seasonal organophosphate/carbamate exposure was investigated for the tropical scallop, Euvola (Pecten) ziczac [11].
  • The Phe-Met-Arg-Phe NH2 (FMRFamide)-like immunoreactivity was detected in neurons of the cerebro-pedal and visceral ganglia of the scallop Pecten maximus using immunohistochemical techniques [12].
 

Associations of Pecten with chemical compounds

  • Scallops, Pecten maximus, accumulate cadmium naturally in the digestive gland to a level of approximately 100 ppm wet weight [13].
  • Under aerobic conditions, or in retinas placed directly into fixative, retinal samples from the central edge of the pecten did not show differential cellular staining for aspartate [14].
  • Two PCR-RFLP mitochondrial DNA (mtDNA) markers were developed through the cloning and sequencing of mtDNA from the scallop Pecten maximus, and were used to study genetic differentiation off UK and Atlantic coast populations of this species [15].
  • Changes in sterol composition of Pecten maximus larvae during the larval development stage with standard algal mixtures and unialgal diets were analysed [16].
  • Purification and properties of two molecular forms of arginine kinase from the adductor muscle of the scallop, Pecten maximus [17].
 

Gene context of Pecten

  • Only a small decrease in the expression of VEGF and Ang-2 was detected in the pecten oculi upon inhibition of the proteasome, while no major changes were observed in the expression of other angiogenic molecules, such as KDR or Ang-1 [18].
  • The method was validated for the quantitative detection of OA, YTX, PTX-2, and AZA-1 in 4 species (mussels, Mytilus edulis; cockles, Cerastoderma edule; oysters, Crassostrea gigas; king scallop, Pecten maximus) of shellfish obtained from United Kingdom (UK) waters [19].
  • 1. Two molecular forms of arginine kinase, AK1 and AK2 have been purified from the adductor muscle of the scallop, Pecten maximus [17].
  • Target organs for calcitonin gene-related peptide (CGRP) were investigated in Pecten maximus using 125I-labelled human CGRP [20].
  • Characterisation of the bacterial community associated with early stages of Great Scallop (Pecten maximus), using denaturing gradient gel electrophoresis (DGGE) [21].
 

Analytical, diagnostic and therapeutic context of Pecten

  • Two types (isoenzymes) of octopine dehydrogenase (A and B) from Pecten jacobaeus adductor muscle were purified to homogeneity, applying affinity chromatography as an efficient final step of purification [22].

References

  1. The role of bone morphogenetic proteins in the differentiation of the ventral optic cup. Adler, R., Belecky-Adams, T.L. Development (2002) [Pubmed]
  2. Primary structure of myosin from the striated adductor muscle of the Atlantic scallop, Pecten maximus, and expression of the regulatory domain. Janes, D.P., Patel, H., Chantler, P.D. J. Muscle Res. Cell. Motil. (2000) [Pubmed]
  3. A folded (10 S) conformer of myosin from a striated muscle and its implications for regulation of ATPase activity. Ankrett, R.J., Rowe, A.J., Cross, R.A., Kendrick-Jones, J., Bagshaw, C.R. J. Mol. Biol. (1991) [Pubmed]
  4. R- and B-cadherin expression defines subpopulations of glial cells involved in axonal guidance in the optic nerve head of the chicken. Gerhardt, H., Rascher, G., Schuck, J., Weigold, U., Redies, C., Wolburg, H. Glia (2000) [Pubmed]
  5. Fluorescence studies on the nucleotide- and Ca2+-binding domains of molluscan myosin. Wells, C., Warriner, K.E., Bagshaw, C.R. Biochem. J. (1985) [Pubmed]
  6. Octopine dehydrogenase from Pecten maximus: steady-state mechanism. Schrimsher, J.L., Taylor, K.B. Biochemistry (1984) [Pubmed]
  7. Isolation of Hox and ParaHox genes in the bivalve Pecten maximus. Canapa, A., Biscotti, M.A., Olmo, E., Barucca, M. Gene (2005) [Pubmed]
  8. Seasonal changes in lipid classes and fatty acid composition in the digestive gland of Pecten maximus. Pazos, A.J., Sánchez, J.L., Román, G., Luz Pérez-Parallé, M., Abad, M. Comp. Biochem. Physiol. B, Biochem. Mol. Biol. (2003) [Pubmed]
  9. N-cadherin expression in endothelial cells during early angiogenesis in the eye and brain of the chicken: relation to blood-retina and blood-brain barrier development. Gerhardt, H., Liebner, S., Redies, C., Wolburg, H. Eur. J. Neurosci. (1999) [Pubmed]
  10. The prolonged hyperpolarizing afterpotential in an invertebrate photoreceptor: wavelength and ionic dependence. Cornwall, M.C., Gorman, A.L. Brain Res. (1982) [Pubmed]
  11. An evaluation of hemolymph cholinesterase activities in the tropical scallop, Euvola (Pecten) ziczac, for the rapid assessment of pesticide exposure. Owen, R., Buxton, L., Sarkis, S., Toaspern, M., Knap, A., Depledge, M. Mar. Pollut. Bull. (2002) [Pubmed]
  12. Immunohistochemical localization of FMRFamide-containing neurons and nerve fibers in the ganglia and the gonad wall of the scallop, Pecten maximus (L). Henry, M., Benlinmame, N., Belhsen, O.K., Jule, Y., Mathieu, M. Neuropeptides (1995) [Pubmed]
  13. Cadmium-binding proteins in the scallop Pecten maximus. Stone, H.C., Wilson, S.B., Overnell, J. Environ. Health Perspect. (1986) [Pubmed]
  14. Glutamate metabolic pathways in displaced ganglion cells of the chicken retina. Kalloniatis, M., Napper, G.A. J. Comp. Neurol. (1996) [Pubmed]
  15. Mitochondrial DNA variation in the scallop Pecten maximus (L.) assessed by a PCR-RFLP method. Wilding, C.S., Beaumont, A.R., Latchford, J.W. Heredity (1997) [Pubmed]
  16. Incorporation of microalgae sterols by scallop Pecten maximus (L.) larvae. Soudant, P., Le Coz, J.R., Marty, Y., Moal, J., Robert, n.u.l.l., Samain, J.F. Comp. Biochem. Physiol., Part A Mol. Integr. Physiol. (1998) [Pubmed]
  17. Purification and properties of two molecular forms of arginine kinase from the adductor muscle of the scallop, Pecten maximus. Reddy, S.R., Roustan, C., Benyamin, Y. Comp. Biochem. Physiol., B (1991) [Pubmed]
  18. Down-regulation of Flt-1 gene expression by the proteasome inhibitor MG262. Mezquita, J., Mezquita, B., Pau, M., Mezquita, C. J. Cell. Biochem. (2003) [Pubmed]
  19. Liquid chromatography with mass spectrometry--detection of lipophilic shellfish toxins. Stobo, L.A., Lacaze, J.P., Scott, A.C., Gallacher, S., Smith, E.A., Quilliam, M.A. Journal of AOAC International. (2005) [Pubmed]
  20. Characterization of binding sites for calcitonin gene-related peptide in the mollusc gill. Fouchereau-Peron, M. Regul. Pept. (1996) [Pubmed]
  21. Characterisation of the bacterial community associated with early stages of Great Scallop (Pecten maximus), using denaturing gradient gel electrophoresis (DGGE). Sandaa, R.A., Magnesen, T., Torkildsen, L., Bergh, O. Syst. Appl. Microbiol. (2003) [Pubmed]
  22. Isolation, physicochemical properties, and folding of octopine dehydrogenase from Pecten jacobaeus. Zettlmeissl, G., Teschner, W., Rudolph, R., Jaenicke, R., Gäde, G. Eur. J. Biochem. (1984) [Pubmed]
 
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