TY - JOUR
T1 - 3pK, a new mitogen-activated protein kinase-activated protein kinase located in the small cell lung cancer tumor suppressor gene region
AU - Sithanandam, Gunamani
AU - Latif, Farida
AU - Duh, Fuh Mei
AU - Bernal, Ricardo
AU - Smola, Ute
AU - Li, Hua
AU - Kuzmin, Igor
AU - Wixler, Viktor
AU - Geil, Laura
AU - Shrestha, Sadeep
AU - Lloyd, Patricia A.
AU - Bader, Scott
AU - Sekido, Yoshitaka
AU - Tartof, Kenneth D.
AU - Kashuba, Vladimir I.
AU - Zabarovsky, Eugene R.
AU - Dean, Michael
AU - Klein, George
AU - Lerman, Michael I.
AU - Minna, John D.
AU - Rapp, Ulf R.
AU - Allikmets, Rando
PY - 1996/3
Y1 - 1996/3
N2 - NotI linking clones, localized to the human chromosome 3p21.3 region and homozygously deleted in small cell lung cancer cell lines NCI-H740 and NCI- H1450, were used to search for a putative tumor suppressor gene(s). One of these clones, NL1G210, detected a 2.5-kb mRNA in all examined human tissues, expression being especially high in the heart and skeletal muscle. Two overlapping cDNA clones containing the entire open reading frame were isolated from a human heart cDNA library and fully characterized. Computer analysis and a search of the GenBank database revealed high sequence identity of the product of this gene to serine-threonine kinases, especially to mitogen-activated protein kinase-activated protein kinase 2, a recently described substrate of mitogen-activated kinases. Sequence identity was 72% at the nucleotide level and 75% at the amino acid level, strongly suggesting that this protein is a serine-threonine kinase. Here we demonstrate that the new gene, referred to as 3pK (for chromosome 3p kinase), in fact encodes a mitogen-activated protein kinase-regulated protein serine-threonine kinase with a novel substrate specificity.
AB - NotI linking clones, localized to the human chromosome 3p21.3 region and homozygously deleted in small cell lung cancer cell lines NCI-H740 and NCI- H1450, were used to search for a putative tumor suppressor gene(s). One of these clones, NL1G210, detected a 2.5-kb mRNA in all examined human tissues, expression being especially high in the heart and skeletal muscle. Two overlapping cDNA clones containing the entire open reading frame were isolated from a human heart cDNA library and fully characterized. Computer analysis and a search of the GenBank database revealed high sequence identity of the product of this gene to serine-threonine kinases, especially to mitogen-activated protein kinase-activated protein kinase 2, a recently described substrate of mitogen-activated kinases. Sequence identity was 72% at the nucleotide level and 75% at the amino acid level, strongly suggesting that this protein is a serine-threonine kinase. Here we demonstrate that the new gene, referred to as 3pK (for chromosome 3p kinase), in fact encodes a mitogen-activated protein kinase-regulated protein serine-threonine kinase with a novel substrate specificity.
UR - http://www.scopus.com/inward/record.url?scp=9044220225&partnerID=8YFLogxK
U2 - 10.1128/MCB.16.3.868
DO - 10.1128/MCB.16.3.868
M3 - Article
C2 - 8622688
AN - SCOPUS:9044220225
SN - 0270-7306
VL - 16
SP - 868
EP - 876
JO - Molecular and Cellular Biology
JF - Molecular and Cellular Biology
IS - 3
ER -