Artículos de revistas
PIP4KIIA and beta-globin: transcripts differentially expressed in reticulocytes and associated with high levels of Hb H in two siblings with Hb H disease
Registro en:
European Journal Of Haematology. Wiley-blackwell, v. 83, n. 5, n. 490, n. 493, 2009.
0902-4441
WOS:000270650700012
10.1111/j.1600-0609.2009.01325.x
Autor
Wenning, MRSC
Mello, MP
Andrade, TG
Lanaro, C
Albuquerque, DM
Saad, STO
Costa, FF
Sonati, MF
Institución
Resumen
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) We are reporting here the results of differential gene expression experiments comparing two siblings, a 21-yr-old male and a 19-yr-old female, with the same alpha-thalassemia genotype (-alpha 3.7/--SEA) and quite different levels of Hb H in the peripheral blood (18.7 and 5%, respectively). By using mRNA differential-display reverse-transcription-PCR and suppression subtractive hybridization, two main transcripts were selected in both procedures and validated by qRT-PCR, one corresponding to the phosphatidylinositol phosphate 4-kinase type II-alpha (PIP4KIIA) gene and the other to the beta-globin gene, both over expressed in the patient with the higher percentage of Hb H. Type II PIP kinases produce phosphatidylinositol 4,5 biphosphate, a critical and pleiotropic regulatory molecule involved in diverse cellular activities, including gene expression. Our results suggest that PIP4KIIA may be one of the factors related to the regulation of the beta-globin gene expression and the different levels of Hb H in alpha-thalassemic patients. 83 5 490 493 Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) FAPESP [02/13801-7]