Source:http://linkedlifedata.com/resource/pubmed/id/17600970
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions |
umls-concept:C0004561,
umls-concept:C0017262,
umls-concept:C0183683,
umls-concept:C0185117,
umls-concept:C0206414,
umls-concept:C0344211,
umls-concept:C0449774,
umls-concept:C0542341,
umls-concept:C1171411,
umls-concept:C1317973,
umls-concept:C1335193,
umls-concept:C1521721,
umls-concept:C1955829,
umls-concept:C2003939,
umls-concept:C2911684
|
pubmed:issue |
12
|
pubmed:dateCreated |
2007-6-29
|
pubmed:abstractText |
The transcription factor Pax5 is essential for B cell commitment and development. Although the detail Pax5 expression pattern within the hemopoietic system is still largely unknown, we previously reported that Pax5 is monoallelically transcribed in pro-B and mature B cells. In this study, we have investigated the expression of Pax5 at single-cell resolution by inserting a GFP or human Cd2 indicator gene under the translational control of an internal ribosomal entry sequence into the 3' untranslated region of Pax5. These insertions were noninvasive, as B cell development was normal in Pax5(ihCd2/ihCd2) and Pax5(ihGFP/iGFP) mice. Transheterozygous Pax5(ihCd2/iGFP) mice coexpressed GPF and human CD2 at similar levels from pro-B to mature B cells, thus demonstrating biallelic expression of Pax5 at all stages of B cell development. No reporter gene expression could be detected in plasma cells and non-B cells of hemopoietic system. Moreover, the vast majority of common lymphoid progenitors and pre-pro-B in the bone marrow of Pax5(ihGFP/iGFP) mice did not yet express GFP, indicating that Pax5 expression is fully switched on only during the transition form uncommitted pre-pro-B cells to committed pro-B cells. Hence, the transcriptional initiation and B cell-specific expression of Pax5 is entirely consistent with its B cell lineage commitment function.
|
pubmed:commentsCorrections | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD2,
http://linkedlifedata.com/resource/pubmed/chemical/B-Cell-Specific Activator Protein,
http://linkedlifedata.com/resource/pubmed/chemical/Green Fluorescent Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Pax5 protein, mouse
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
0022-1767
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
178
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
8222-8
|
pubmed:meshHeading |
pubmed-meshheading:17600970-Alleles,
pubmed-meshheading:17600970-Animals,
pubmed-meshheading:17600970-Antigens, CD2,
pubmed-meshheading:17600970-B-Cell-Specific Activator Protein,
pubmed-meshheading:17600970-B-Lymphocytes,
pubmed-meshheading:17600970-Gene Expression Regulation,
pubmed-meshheading:17600970-Genes, Reporter,
pubmed-meshheading:17600970-Green Fluorescent Proteins,
pubmed-meshheading:17600970-Hematopoietic Stem Cells,
pubmed-meshheading:17600970-Humans,
pubmed-meshheading:17600970-Lymphocyte Activation,
pubmed-meshheading:17600970-Mice,
pubmed-meshheading:17600970-Mice, Knockout,
pubmed-meshheading:17600970-Plasma Cells
|
pubmed:year |
2007
|
pubmed:articleTitle |
Reporter gene insertions reveal a strictly B lymphoid-specific expression pattern of Pax5 in support of its B cell identity function.
|
pubmed:affiliation |
Research Institute of Molecular Pathology, Vienna Biocenter, Austria.
|
pubmed:publicationType |
Journal Article,
Comment,
Research Support, Non-U.S. Gov't
|