2 results
Differential Response of Liverwort (Marchantia polymorpha) Tissue to POST-Applied Quinoclamine
- James E. Altland, Glenn Wehtje, Jeff Sibley, Michael E. Miller, Charles H. Gilliam, Charles Krause
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- Journal:
- Weed Technology / Volume 25 / Issue 4 / December 2011
- Published online by Cambridge University Press:
- 20 January 2017, pp. 580-585
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Quinoclamine is used in Europe, and was under evaluation in the Unites States for the control of liverwort in nursery crops. Liverwort is a nonvascular, chlorophyll-containing plant that can be problematic in greenhouse and nursery crops. POST-applied quinoclamine controls liverwort. However, liverwort structures vary in their sensitivity to POST-applied quinoclamine. Specifically, archegonial receptacles (female) are much more tolerant of quinoclamine than either antheridial receptacles (male) or thalli (leaflike structures). A series of studies were conducted to, first, document the degree of differential sensitivity between tissues to quinoclamine, and second, to determine the basis of this differential sensitivity. The dose that results in 50% of the population being controlled (I50) of antheridial receptacles and juvenile thalli were estimated to be 1.60 and 1.27 kg·ha−1, respectively. The I50 of archegonial receptacles could not be estimated, but exceeded 10.45 kg·ha−1. Chlorophyll content varied between liverwort tissues, but the content did not correlate to quinoclamine sensitivity. Absorption of 14C after application of radiolabeled quinoclamine was less in archegonial receptacles than in either antheridial receptacles or thalli. Scanning electron microscopy of the surface of the liverwort tissues revealed that archegonial receptacles had smaller pores (equivalent to stomata in higher plants) than either antheridial receptacles or thalli. The tolerance of archegonial receptacles to quinoclamine can be partially, but not exclusively, attributed to reduced absorption. This reduced absorption may be attributed to the limited pore size and less total pore area of the archegonial receptacles.
Expression and cellular localization of substance P/neurokinin A and neurokinin B mRNAs in the rat retina
- Nicholas C. Brecha, Catia Sternini, Karl Anderson, James E. Krause
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- Journal:
- Visual Neuroscience / Volume 3 / Issue 6 / December 1989
- Published online by Cambridge University Press:
- 02 June 2009, pp. 527-535
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The mammalian tachykinin peptides, substance P (SP), neurokinin A (NKA), and neurokinin B (NKB) are encoded by distinct mRNAs derived from separate preprotachykinin (PPT) genes. The SP/NKA-encoding PPT gene generates three mRNAs by alternative RNA processing: α-PPT mRNA, which encodes SP only, and β- and γ-PPT mRNAs, which encode both SP and NKA. The NKB-encoding PPT gene generates mRNAs that produce NKB. The distribution and cellular localization of SP, NKA and NKB mRNAs in the rat retina were studied by RNA blot and in situ hybridization techniques. Blot hybridization analysis of retinal RNA extracts with [32P]-labeled RNA probes complementary to SP/NKA and NKB mRNAs demonstrated single bands of hybridization at 1300 and 900 bases, respectively. Solution hybridization-nuclease protection experiments showed multiple SP/NKA-encoding transcripts with relative levels of ρ-PPT mRNA > β-PPT mRNA ≫ α-PPT mRNA. In situ hybridization histochemistry with [35S]-labeled antisense RNAs demonstrated thatSP/NKA-encoding transcripts are expressed in small-to-medium somata located in the proximal inner nuclear, inner plexiform, and ganglion cell layers, whereas NKB-encoding transcripts are expressed in small-to-medium somata located only in the ganglion cell layer. In this layer, cells containing NKB mRNAs are more numerous than those containing SP/NKA mRNAs. Only background labeling was observed in sections incubated with sense RNA probes, pretreated with RNase A prior to hybridization or incubated in hybridization buffer without the labeled probe. Immunohistochemical studies with a monoclonal antibody directed to the conserved COOH-terminal sequence of the tachykinin peptides revealed tachykinin-like immunoreactive somata with similar size and distribution to those containing SP/NKA- and NKB-encoding transcripts. These results indicate that both SP/NKA and NKB mRNAs are present in the rat retina and that the PPT genes are differentially expressed in specific cell populations. The size and distribution of these cells suggest that they are amacrine and displaced amacrine cells, however, the possibility that tachykinins are present also in ganglion cells in the rat retina cannot be ruled out.