TY - JOUR
T1 - ABL and BCR Genes are not imprinted in androgenetic and gynogenetic human tissues
AU - Lorberboum-Galski, Haya
AU - Yarkoni, Shai
AU - Nechushtan, Amotz
AU - Rachmilewitz, Jacob
AU - De Groot, Nathan
AU - Hochberg, Abraham
PY - 1994/10/31
Y1 - 1994/10/31
N2 - In the translocation leading to the formation of the Philadelphia chromosome, the hallmark of chronic myeloid leukemia (CML), the translocated chromosome 9 (ABL), is of paternal descent whereas chromosome 22 (BCR) is of maternal origin (1). To study possible imprinting of the human ABL and BCR genes, we used human tissues exclusively endowed with their maternally (benign teratoma) or paternally (complete hydatidiform mole) inherited chromosomes. Using the sensitive PCR technique followed by northern blotting, we demonstrate here that ABL and BCR are expressed to a similar extent in androgenetic and gynogenetic human tissues, thus suggesting that ABL and BCR genes are not imprinted in these human tissues.
AB - In the translocation leading to the formation of the Philadelphia chromosome, the hallmark of chronic myeloid leukemia (CML), the translocated chromosome 9 (ABL), is of paternal descent whereas chromosome 22 (BCR) is of maternal origin (1). To study possible imprinting of the human ABL and BCR genes, we used human tissues exclusively endowed with their maternally (benign teratoma) or paternally (complete hydatidiform mole) inherited chromosomes. Using the sensitive PCR technique followed by northern blotting, we demonstrate here that ABL and BCR are expressed to a similar extent in androgenetic and gynogenetic human tissues, thus suggesting that ABL and BCR genes are not imprinted in these human tissues.
UR - http://www.scopus.com/inward/record.url?scp=0028004392&partnerID=8YFLogxK
U2 - 10.1006/bbrc.1994.2504
DO - 10.1006/bbrc.1994.2504
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C2 - 7980523
AN - SCOPUS:0028004392
SN - 0006-291X
VL - 204
SP - 621
EP - 627
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -