Fig. 1.
Fig. 1. Up-regulation of transcription factor and signal transduction genes in HTLV-1–infected T lymphocytes. / Total RNA was isolated from HTLV-1+/Tax+(C91-PL, HuT-102, MT-2, TAXI-1, JuanaW) and HTLV-1−/Tax− cell cultures (PBMCPHA, HuT-78, Jurkat), separated on denaturing gels, and subjected to Northern blot analysis. Specific mRNAs of the expected sizes were detected by radioactively labeled cDNAs derived from the transcription factor DEC-1, and signal transduction genes (PAC1, B94, ferritin L-chain, ISG15, and calcyclin). Some of the genes were found to be consistently up-regulated in all Tax+ cells (A); others were preferentially up-regulated in ATL patient-derived cultures (B). Equal RNA loading was controlled by hybridization to an internal standard (GAPDH). Results are representative of 3 independent Northern blots. J indicates JuanaW RNA; P, PBMCPHA RNA. The size of the transcripts is indicated in brackets. *For the B94 expression analysis MT-2 RNA was used instead of HuT-102 RNA.

Up-regulation of transcription factor and signal transduction genes in HTLV-1–infected T lymphocytes.

Total RNA was isolated from HTLV-1+/Tax+(C91-PL, HuT-102, MT-2, TAXI-1, JuanaW) and HTLV-1/Tax cell cultures (PBMCPHA, HuT-78, Jurkat), separated on denaturing gels, and subjected to Northern blot analysis. Specific mRNAs of the expected sizes were detected by radioactively labeled cDNAs derived from the transcription factor DEC-1, and signal transduction genes (PAC1, B94, ferritin L-chain, ISG15, and calcyclin). Some of the genes were found to be consistently up-regulated in all Tax+ cells (A); others were preferentially up-regulated in ATL patient-derived cultures (B). Equal RNA loading was controlled by hybridization to an internal standard (GAPDH). Results are representative of 3 independent Northern blots. J indicates JuanaW RNA; P, PBMCPHA RNA. The size of the transcripts is indicated in brackets. *For the B94 expression analysis MT-2 RNA was used instead of HuT-102 RNA.

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