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Changes in replication, nuclear location, and expression of the Igh locus after fusion of a pre-B cell line with a T cell line.
Zhou, Jie; Saleque, Shireen; Ermakova, Olga; Sepulveda, Manuel A; Yang, Qiaoxin; Eckhardt, Laurel A; Schildkraut, Carl L; Birshtein, Barbara K.
Afiliação
  • Zhou J; Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
J Immunol ; 175(4): 2317-20, 2005 Aug 15.
Article em En | MEDLINE | ID: mdl-16081801
ABSTRACT
We have previously observed that replication and nuclear location of the murine Igh locus are developmentally regulated during B cell differentiation. In non-B, B, and plasma cells, sequences near the 3' end of the Igh locus replicate early in S while upstream Vh sequences replicate late in S, and the Igh locus is located near the nuclear periphery. In fact, in MEL non-B cells, replication of a 500-kb segment containing Igh-C and flanking sequences occurs progressively later throughout S by 3' to 5' unidirectional fork movement. In contrast, in pro- and pre-B cells, the entire 3-Mb Igh locus is located away from the nuclear periphery and replicates early in S by forks progressing in both directions. In this study, using an 18-81 (pre-B) x BW5147 (T) cell fusion system in which Igh expression is extinguished, we found that in all Igh alleles, Vh sequences replicated later in S than 3' Igh sequences (similar to that detected in BW5147), but the Igh locus was situated away from the nuclear periphery (similar to that observed in 18-81). Thus, pre-B cell-derived Igh genes had changes in replication timing, but not in nuclear location, whereas T cell-derived Igh genes changed their nuclear location but not their replication timing. These data are consistent with the silencing of a pre-B cell-specific replication program in the fusion hybrid cells and independent regulation of the nuclear location of Igh loci.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Células-Tronco Hematopoéticas / Linfócitos B / Linfócitos T / Núcleo Celular / Cadeias Pesadas de Imunoglobulinas / Replicação do DNA / Células Híbridas Limite: Animals Idioma: En Revista: J Immunol Ano de publicação: 2005 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Células-Tronco Hematopoéticas / Linfócitos B / Linfócitos T / Núcleo Celular / Cadeias Pesadas de Imunoglobulinas / Replicação do DNA / Células Híbridas Limite: Animals Idioma: En Revista: J Immunol Ano de publicação: 2005 Tipo de documento: Article País de afiliação: Estados Unidos