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Mcm3ap  -  minichromosome maintenance deficient 3 (S....

Mus musculus

Synonyms: GANP, GC-associated DNA primase, Ganp, Germinal-center associated nuclear protein, Map80, ...
 
 
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Disease relevance of Mcm3ap

  • These results suggest that GANP overexpression is a causative factor in the generation of B lymphomas [1].
 

High impact information on Mcm3ap

  • G5PR associates with GANP, whose expression is up-regulated in mature B cells of the peripheral lymphoid organs [2].
  • B cell-specific ganp-deficient mice showed a decreased frequency of variable-region somatic mutations, especially of the high-affinity type (W(33) --> L) in the V(H)186.2 region against nitrophenyl-chicken gamma globulin, whereas the class switching was normal [3].
  • A novel nuclear phosphoprotein, GANP, is up-regulated in centrocytes of the germinal center and associated with MCM3, a protein essential for DNA replication [4].
  • The expression of GANP was strikingly correlated with GC formation because Bcl6-deficient mice did not show the up-regulation of GANP [4].
  • GANP is a 210-kd protein localized in both the cytoplasm and nuclei, with a homologous region to Map80 that is associated with MCM3, a protein essential for DNA replication [4].
 

Biological context of Mcm3ap

  • In the study reported here, we have shown abnormal up-regulation of germinal center B cell-associated GANP in various human lymphomas including mantle cell, diffuse large B cell, and Hodgkin lymphoma, by immunohistochemical analysis [1].
  • To study the role of GANP in lymphomagenesis, we generated mutant mice (ganp-Tg) that express the transgenic ganp gene under immunoglobulin enhancer and promoter control [1].
  • Germinal center-associated DNA primase (GANP) associated with MCM3 of the DNA replication complex is up-regulated selectively in germinal center B cells [5].
  • Selective regulation of ganp expression was observed in the -737-bp promoter region in B and plasma cell lines but was significantly low in pre-B and T cell lines [5].
  • GANP-positive cells appeared in the light zone of the GC, with coexpression of the peanut agglutinin (PNA) (PNA)-positive B220-positive phenotype [4].
 

Anatomical context of Mcm3ap

 

Other interactions of Mcm3ap

  • GANP promoter activity was higher in wild-type vs Lyn-deficient cells [7].

References

  1. Increased expression of germinal center-associated nuclear protein RNA-primase is associated with lymphomagenesis. Fujimura, S., Xing, Y., Takeya, M., Yamashita, Y., Ohshima, K., Kuwahara, K., Sakaguchi, N. Cancer Res. (2005) [Pubmed]
  2. Protein phosphatase subunit G5PR is needed for inhibition of B cell receptor-induced apoptosis. Xing, Y., Igarashi, H., Wang, X., Sakaguchi, N. J. Exp. Med. (2005) [Pubmed]
  3. Germinal center-associated nuclear protein contributes to affinity maturation of B cell antigen receptor in T cell-dependent responses. Kuwahara, K., Fujimura, S., Takahashi, Y., Nakagata, N., Takemori, T., Aizawa, S., Sakaguchi, N. Proc. Natl. Acad. Sci. U.S.A. (2004) [Pubmed]
  4. A novel nuclear phosphoprotein, GANP, is up-regulated in centrocytes of the germinal center and associated with MCM3, a protein essential for DNA replication. Kuwahara, K., Yoshida, M., Kondo, E., Sakata, A., Watanabe, Y., Abe, E., Kouno, Y., Tomiyasu, S., Fujimura, S., Tokuhisa, T., Kimura, H., Ezaki, T., Sakaguchi, N. Blood (2000) [Pubmed]
  5. PU.1 is involved in the regulation of B lineage-associated and developmental stage-dependent expression of the germinal center-associated DNA primase GANP. EL-Gazzar, M.A., Maeda, K., Nomiyama, H., Nakao, M., Kuwahara, K., Sakaguchi, N. J. Biol. Chem. (2001) [Pubmed]
  6. Spontaneous increase of plasma-like cells with high GANP expression in the extrafollicular region of lymphoid organs of autoimmune-prone mice. Fujimura, S., Kuwahara, K., Ezaki, T., Tomita, K., Hirose, S., Sakaguchi, N. J. Autoimmun. (2003) [Pubmed]
  7. Microarray analysis of Lyn-deficient B cells reveals germinal center-associated nuclear protein and other genes associated with the lymphoid germinal center. Mirnics, Z.K., Caudell, E., Gao, Y., Kuwahara, K., Sakaguchi, N., Kurosaki, T., Burnside, J., Mirnics, K., Corey, S.J. J. Immunol. (2004) [Pubmed]
 
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