<?xml version="1.0"?>
<Articles JournalTitle="Journal of Arthropod-Borne Diseases">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Journal of Arthropod-Borne Diseases</JournalTitle>
      <Issn>2322-1984</Issn>
      <Volume>2</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2008</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Cloning and Expression of TRYP6 Gene from Leishmania major (MRHO/IR/75/ER)</title>
    <FirstPage>7</FirstPage>
    <LastPage>15</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>G</FirstName>
        <LastName>Eslami</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>R</FirstName>
        <LastName>Salehi</LastName>
        <affiliation locale="en_US">Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sci- ences, Isfahan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>H</FirstName>
        <LastName>Hejazi</LastName>
        <affiliation locale="en_US">Department of Parasitology and Mycology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>A</FirstName>
        <LastName>Khamesipour</LastName>
        <affiliation locale="en_US">Center for Research and Training in Skin Diseases and Leprosy, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>B</FirstName>
        <LastName>Kazemi</LastName>
        <affiliation locale="en_US">Cellular and Molecular Biology Research Center, Department of Parasitology, School of Medicine, Sha-&#xD;
heed Beheshti University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>03</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: Leishmania, needs to detoxify the macrophage derived potent peroxides (H2O2). Tryparedoxin path&#xAD;way contains tryparedoxin peroxidase (TSA or TRYP). The aim of the study was to detect the full-length gene se&#xAD;quence and its encoded protein of the LmTRYP6 gene (EU251502), and comparison the gene sequence with LmTRYP6 (LmjF15.1140), another previously reported member of this gene family.
Methods: L.major (MRHO/IR/75/ER) promastigotes were cultured, DNA and RNA were extracted and the inter&#xAD;ested gene was amplified using PCR and RT-PCR methods.&#xA0; PCR/ RT-PCR fragments were purified and cloned first in pTZ57R/T and then in pET15b expression vector. The expressed protein was verified using western blot method. Char&#xAD;acterization of the expressed protein was performed bioinformatically.
Results: Molecular evaluation revealed that the cloned LmTRYP6 gene (EU251502) encoded a predicted 184 amino acid long protein with a theoretical isoelectric point of 6.1101. Alignment showed a number of changes in amino acid composition including the replacement of highly conserved Trp177 by Cys in LmTRYP6 (ABX26130).
Conclusion: So far no study has been done on this group, i.e. &#xA0;TRYP6 gene, from tryparedoxin peroxidase family. The low homology with LmTRYP6 (LmjF15.1140) and vast array of differences observed in the gene under study (LmTRYP6; EU251502) could open new windows in the field of anti-Leishmania combat. Based on its important role in the viability and successful establishment of the parasite in the host organism it looks to be very good candi&#xAD;date for vaccine development and any other sort of novel drug development.</abstract>
    <web_url>https://jad.tums.ac.ir/index.php/jad/article/view/21</web_url>
    <pdf_url>https://jad.tums.ac.ir/index.php/jad/article/download/21/19</pdf_url>
  </Article>
</Articles>
