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FLRG (follistatin-related gene), a new target of chromosomal rearrangement in malignant blood disorders.
Hayette, S; Gadoux, M; Martel, S; Bertrand, S; Tigaud, I; Magaud, J P; Rimokh, R.
Afiliação
  • Hayette S; Laboratoire de Cytogénétique Moléculaire, Hopital Edouard Herriot, Lyon, France.
Oncogene ; 16(22): 2949-54, 1998 Jun 04.
Article em En | MEDLINE | ID: mdl-9671416
ABSTRACT
We report here the molecular study of a t(11;19)(q13;p13) translocation observed in a case of B-cell chronic lymphocytic leukemia. This translocation leads to the juxtaposition of the CCND1 gene on chromosome 11 to a new transcriptional unit on chromosome 19. The cDNA of this new evolutionarily conserved gene (named FLRG for Follistatin-Related Gene) codes for a secreted glycoprotein of the follistatin-module-protein family. FLRG is expressed in a wide range of human and murine adult tissues and its expression seems to be tightly regulated during murine embryogenesis. Its transcripts could not be detected in hematopoietic cells from all lineages and in particular in cells from lymphoid B and T lineage except in the t(11;19)-carrying leukemia described here. A great variability of expression is observed among the other tumoral cell lines analysed. Besides the t(11;19)-carrying leukemia described in this work, structural rearrangements of the FLRG locus have been found in a non-Hodgkin lymphoma, suggesting that it may play a role in leukemogenesis.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Translocação Genética / Cromossomos Humanos Par 11 / Cromossomos Humanos Par 19 / Glicoproteínas / Leucemia Linfocítica Crônica de Células B / Ciclina D1 Limite: Animals / Humans Idioma: En Revista: Oncogene Assunto da revista: BIOLOGIA MOLECULAR / NEOPLASIAS Ano de publicação: 1998 Tipo de documento: Article País de afiliação: França
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Translocação Genética / Cromossomos Humanos Par 11 / Cromossomos Humanos Par 19 / Glicoproteínas / Leucemia Linfocítica Crônica de Células B / Ciclina D1 Limite: Animals / Humans Idioma: En Revista: Oncogene Assunto da revista: BIOLOGIA MOLECULAR / NEOPLASIAS Ano de publicação: 1998 Tipo de documento: Article País de afiliação: França