Literature DB >> 10826697

cDNA cloning of lymphotoxin alpha (LT-alpha) from a marsupial, Macropus eugenii.

G A Harrison1, E M Deane.   

Abstract

Lymphotoxin (LT) is a proinflammatory cytokine with a broad spectrum of immunological activities. While the 'classic' form of the molecule is a secreted homotrimer, now referred to in the literature as LT-alpha3, it has more recently been recognised that a membrane-bound form of LT exists on activated T lymphocytes and that this represents a complex between LT-alpha and a closely related type II membrane protein, LT-beta. Together with another related cytokine, tumour necrosis factor alpha (TNF-alpha), these molecules have been extremely well studied in eutherian mammals but not in any other group. Marsupials represent a distinct branch in mammalian evolution to that of eutherians, the two groups having diverged more than 100 million years ago. We report here for the first time, the cDNA cloning of LT-alpha from a marsupial, Macropus eugenii (tammar wallaby). This sequence was found to be relatively conserved when compared to orthologous sequences from eutherian mammals, sharing an average sequence identity of 70.4% at the nucleotide level and 71.7% at the deduced amino acid level.

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Year:  2000        PMID: 10826697     DOI: 10.3109/10425170009015608

Source DB:  PubMed          Journal:  DNA Seq        ISSN: 1026-7913


  3 in total

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Authors:  Emily S W Wong; Anthony T Papenfuss; Katherine Belov
Journal:  BMC Immunol       Date:  2011-08-19       Impact factor: 3.615

2.  In silico identification of opossum cytokine genes suggests the complexity of the marsupial immune system rivals that of eutherian mammals.

Authors:  Emily Sw Wong; Lauren J Young; Anthony T Papenfuss; Katherine Belov
Journal:  Immunome Res       Date:  2006-11-10

3.  Analytical approaches to detect maternal/fetal genotype incompatibilities that increase risk of pre-eclampsia.

Authors:  Neeta Parimi; Gerard Tromp; Helena Kuivaniemi; Jyh Kae Nien; Ricardo Gomez; Roberto Romero; Katrina Ab Goddard
Journal:  BMC Med Genet       Date:  2008-07-03       Impact factor: 2.103

  3 in total

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