Blatt C, Sachs L
Department of Genetics, Weizmann Institute of Science, Rehovot, Israel.
Biochem Biophys Res Commun. 1988 Nov 15;156(3):1265-70. doi: 10.1016/s0006-291x(88)80769-1.
Mouse myeloid leukemias are characterized by a frequent deletion in one chromosome number 2. We now show that there is a deletion of one copy of the Hox-4.1 homeobox gene in the myeloid leukemias with this deletion in chromosome 2. It is suggested that deletion of this homeobox gene plays a role in determining the abnormal developmental program in myeloid leukemia.
小鼠髓性白血病的特征是2号染色体频繁缺失。我们现在表明,在2号染色体发生这种缺失的髓性白血病中,Hox-4.1同源框基因有一个拷贝缺失。有人提出,这个同源框基因的缺失在决定髓性白血病异常发育程序中起作用。