Molecular cloning, structure and bait region splice variants of alpha2-macroglobulin from the soft tick Ornithodoros moubata
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
12878230
DOI
10.1016/s0965-1748(03)00083-3
PII: S0965174803000833
Knihovny.cz E-zdroje
- MeSH
- alfa-makroglobuliny biosyntéza genetika farmakologie MeSH
- DNA primery MeSH
- fylogeneze MeSH
- glykoproteiny MeSH
- hemocyty chemie MeSH
- hmyzí proteiny biosyntéza genetika farmakologie MeSH
- klíšťata genetika MeSH
- klonování DNA MeSH
- komplementární DNA analýza genetika MeSH
- místa sestřihu RNA MeSH
- molekulární sekvence - údaje MeSH
- polymerázová řetězová reakce MeSH
- proteiny členovců MeSH
- regulace genové exprese MeSH
- sekvence aminokyselin MeSH
- sekvence nukleotidů MeSH
- sekvenční analýza DNA MeSH
- slinné žlázy chemie MeSH
- stravovací zvyklosti MeSH
- upregulace MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- alfa-makroglobuliny MeSH
- DNA primery MeSH
- glykoproteiny MeSH
- hmyzí proteiny MeSH
- komplementární DNA MeSH
- místa sestřihu RNA MeSH
- proteiny členovců MeSH
- TAM macroglobulin protein, Ornithodoros moubata MeSH Prohlížeč
The sequence of a alpha(2)-macroglobulin (alpha(2)M) from the soft tick Ornithodoros moubata (TAM) was determined by cloning and sequencing of overlapping polymerase chain reaction (PCR) and rapid amplification of cDNA ends PCR products. The TAM cDNA sequence is 4,944 bp long and contains one open reading frame coding for a protein precursor composed of 1,494 amino-acid residues, including a 24-residue signal sequence. The mature protein is cleaved into two subunits similarly to the C3 and C4 components of complement and fish alpha(2)Ms. Phylogeny analysis revealed that TAM is closely related to Limulus alpha(2)M and displays the highest similarity to the partial sequence of alpha(2)M from hard tick Ixodes scapularis. The comparison of conserved cysteine residues between TAM and human and Limulus alpha(2)Ms made it possible to predict the pattern of disulfide bridges and explain the atypical molecular arrangement of TAM. Four variants of the TAM bait region differing only in a short central segment were found; our data indicate that TAM exists as a single-copy gene in the tick genome and its bait region variants likely arise by alternative splicing. TAM is produced by tick hemocytes and it is also significantly expressed in salivary glands. TAM mRNA levels were shown to be up-regulated upon blood meal.
Citace poskytuje Crossref.org
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GENBANK
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