TY - JOUR
T1 - Unique Pattern of Gene Expression in the Erythroid Precursor Cells
T2 - gene expression/erythroid/CFU‐E/fetal liver
AU - MISHINA, YUJI
AU - KATO, TAKASHI
AU - URABE, AKIO
AU - TAKAKU, FUMIMARO
AU - NATORI, SHUNJI
AU - OBINATA, MASUO
PY - 1986/2
Y1 - 1986/2
N2 - Erythroid cells were fractionated by preformed Percoll density gradient from livers of 12.5 day old mouse fetuses. With combination of lysing of mature erythroid cells, the CFU‐E (colony forming unit of erythroid) was enriched as high as 30% pure. The mRNA levels of the rt‐genes previously cloned as genes expressed in the reticulocytes are estimated in the fractionated erythroid cells. These rt‐genes show a drastic change in expression during erythroid differentiation; Their expression was not detectable at the CFU‐E cell stage. But it reached to maximum at the polychromatic erythroblast (stage I) and then decreases with maturation. The result suggests that mRNA synthesis of these rt‐genes may be induced after the stimulation of erythropoietin.
AB - Erythroid cells were fractionated by preformed Percoll density gradient from livers of 12.5 day old mouse fetuses. With combination of lysing of mature erythroid cells, the CFU‐E (colony forming unit of erythroid) was enriched as high as 30% pure. The mRNA levels of the rt‐genes previously cloned as genes expressed in the reticulocytes are estimated in the fractionated erythroid cells. These rt‐genes show a drastic change in expression during erythroid differentiation; Their expression was not detectable at the CFU‐E cell stage. But it reached to maximum at the polychromatic erythroblast (stage I) and then decreases with maturation. The result suggests that mRNA synthesis of these rt‐genes may be induced after the stimulation of erythropoietin.
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U2 - 10.1111/j.1440-169X.1986.00001.x
DO - 10.1111/j.1440-169X.1986.00001.x
M3 - Article
AN - SCOPUS:0022610610
SN - 0012-1592
VL - 28
SP - 1
EP - 6
JO - Development, growth & differentiation
JF - Development, growth & differentiation
IS - 1
ER -