AI Article Synopsis

  • TET2 is a tumor suppressor gene that, when inactivated, is linked to various hematological cancers and plays a key role in DNA demethylation by converting 5-mC to 5-hmC.
  • The gene has three identified promoters (Pro1, Pro2, Pro3) that produce alternative first exons, with expression varying based on cell type and developmental stage, and showing higher levels in tissues with hematopoietic stem cells like the spleen and bone marrow.
  • Pro2 transcripts are the most widely expressed, while Pro3 is notably present in embryoid bodies but produces a truncated TET2 protein, indicating unique transcriptional regulation mechanisms in both stem cells and differentiated cells.

Article Abstract

Tet methylcytosine dioxygenase 2 () is a tumor suppressor gene that is inactivated in a wide range of hematological cancers. TET2 enzymatic activity converts 5-methylcytosine (5-mC) into 5-hydroxymethylcytosine (5-hmC), an essential step in DNA demethylation. Human TET2 is highly expressed in pluripotent cells and down-regulated in differentiated cells: however, transcriptional regulation of the human gene has not been investigated in detail. Here we define three promoters within a 2.5 kb region located ∼ 87 kb upstream of the first coding exon. The three promoters, designated as Pro1, Pro2, and Pro3, generate three alternative first exons, and their presence in mRNAs varies with cell type and developmental stage. In general, all three transcripts are more highly expressed in human tissues rich in hematopoietic stem cells, such as spleen and bone marrow, compared to other tissues, such as brain and kidney. Transcripts from Pro2 are expressed by a broad range of tissues and at a significantly higher level than Pro1 or Pro3 transcripts. Pro3 transcripts were highly expressed by embryoid bodies generated from the H9 ES cell line, and the major Pro3 transcript is an alternatively spliced mRNA isoform that produces a truncated TET2 protein lacking the catalytic domain. Our study demonstrates distinct tissue-specific mechanisms of transcriptional regulation during early pluripotent states and in differentiated cell types.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6566030PMC
http://dx.doi.org/10.3389/fcell.2019.00099DOI Listing

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