PRELI, the human homologue of the avian px19, is expressed by germinal center B lymphocytes

Liliana Guzman-Rojas, Jennifer C. Sims, Roberto Rangel, Christiane Guret, Yan Sun, Juan M. Alcocer, Hector Martinez-Valdez

Research output: Contribution to journalArticlepeer-review

25 Scopus citations

Abstract

We report the identification of a human cDNA encoding a 25 kDa protein of relevant evolutionary and lymphoid interest (PRELI). PRELI was cloned by screening a B lymphocyte-specific cDNA library with a probe generated by mRNA differential display. PRELI amino acid sequence is 85% similar to the avian px19 protein, expressed within the blood islands and in the liver during avian embryo development. PRELI and px19 contain tandem repeats (A/TAEKAK) of the late embryogenesis abundant (LEA) motif, characteristic of a group of survival molecules and originally thought to be present only in plant proteins. Interestingly, PRELI expression is high in the fetal liver, a major site for B cell lymphopoiesis, while the mRNA levels in other fetal tissues such as the brain, lung, and kidney are comparatively low. At the adult stage, PRELI expression is drastically reduced in the liver but exhibits high mRNA levels in the spleen, brain, lung and kidney tissues, suggesting that PRELI expression may be important for the development of vital and immunocompetent organs. Moreover, PRELI is also highly expressed in the adult lymph nodes and peripheral blood leukocytes, further stressing that at the adult stage, PRELI expression may be important during secondary immune responses. Consistent with this hypothesis, the expression of PRELI is predominant within germinal centers (GC), a stage in which B lymphocytes are under a stressful selection pressure. Taken together these data: (i) strongly support the notion that the conserved LEA motif represents a phylogenetic link between plants and animals, (ii) reveal a novel molecule whose expression may play a role in the maturation of distinct human tissues, and (iii) suggest that PRELI expression may be important for GC B lymphocytes.

Original languageEnglish (US)
Pages (from-to)607-612
Number of pages6
JournalInternational immunology
Volume12
Issue number5
DOIs
StatePublished - 2000

Keywords

  • B lymphocytes
  • Germinal centers
  • LEA motif
  • Phylogeny
  • cDNA cloning

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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