2015
DOI: 10.1016/j.ibmb.2014.11.004
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Tweedle cuticular protein BmCPT1 is involved in innate immunity by participating in recognition of Escherichia coli

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Cited by 28 publications
(18 citation statements)
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References 47 publications
(57 reference statements)
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“…Interestingly, a Twdl gene in B. mori , BmCPT1 , encodes a protein localized to the epicuticle, which also has roles in innate immunity. Overexpression of this gene induces antimicrobial peptide synthesis (Liang et al ., ), suggesting that Twdl proteins have additional roles in insects besides being structural components of the cuticle. These data highlight the developmental utilization of a transcription factor, Ftz‐f1, for distinct developmental events; in this case, moulting/cuticle renewal and immune response.…”
Section: Discussionmentioning
confidence: 99%
“…Interestingly, a Twdl gene in B. mori , BmCPT1 , encodes a protein localized to the epicuticle, which also has roles in innate immunity. Overexpression of this gene induces antimicrobial peptide synthesis (Liang et al ., ), suggesting that Twdl proteins have additional roles in insects besides being structural components of the cuticle. These data highlight the developmental utilization of a transcription factor, Ftz‐f1, for distinct developmental events; in this case, moulting/cuticle renewal and immune response.…”
Section: Discussionmentioning
confidence: 99%
“…Insects are one of the most successful classes of organism, accounting for almost 60% of all described terrestrial species, as a result of their ability to adapt to a wide variety of habitats . Key to their success is the cuticle, which defines body shape and offers protection from environmental stresses such as insecticides, physical injury, dehydration and pathogenic microorganisms. The insect cuticle is primarily composed of cuticular proteins (CPs) and chitin.…”
Section: Introductionmentioning
confidence: 99%
“…The insertion sites of transgenic strains were investigated by using inverse PCR as described previously (Liang et al, 2014;Zhang et al, 2017c). Briefly, the genomic DNA from the G2 transgenic silkworm strains was extracted and treated with proteinase K as well as RNase.…”
Section: Antibody Preparationmentioning
confidence: 99%
“…After digesting with HaeIII, the samples were ligated using T4 DNA ligase for circularization. The PCR amplification was performed as described previously (Liang et al, 2014). All PCR products were cloned into PMD19-T vector (TakaRa) and sequenced at BGI (Beijing, China).…”
Section: Antibody Preparationmentioning
confidence: 99%