TY - JOUR
T1 - Complementary DNA sequence for a 42 kDa rat kidney choline/ethanolamine kinase
AU - Aoyama, C.
AU - Nakashima, K.
AU - Matsui, M.
AU - Ishidate, K.
N1 - Funding Information:
This study was supported in part by Grants-in-Aid (No. 6672173 and No. 8672503) for Scientific Research from the Ministry of Education, Science, Sports and Culture of Japan. K.N. has been supported by Research Fellowships of the Japan Society for the Promotion of Science for Young Scientists. C.A. is a visiting graduate student from Kyoritsu College of Pharmacy, Tokyo.
PY - 1998/2/5
Y1 - 1998/2/5
N2 - By means of peptide sequence information, several cDNA clones encoding a 42 kDa choline/ethanolamine kinase were isolated from a rat kidney cDNA library. Eight clones were sequenced with all of them resulting in identical overlapping nucleotide sequences. Four of them possessed entire open reading frame which could encode 394 amino acids with a calculated molecular size of 45,100. The predicted amino acid sequence contained all of the internal peptide fragment sequences derived from the purified 42 kDa enzyme. When the open reading frame was introduced into pGEX-2T vector and transfected into E. coli cells, a significant choline/ethanolamine kinase activity did appear in the cell lysate. A homology comparison with the previously reported choline kinase cDNAs (CKR1 and CKR2) from rat liver showed 66%-68% in entire nucleotide sequences and 57%-59% in amino acid sequences, indicating that the cloned cDNA here must be a novel CK/EK gene product.
AB - By means of peptide sequence information, several cDNA clones encoding a 42 kDa choline/ethanolamine kinase were isolated from a rat kidney cDNA library. Eight clones were sequenced with all of them resulting in identical overlapping nucleotide sequences. Four of them possessed entire open reading frame which could encode 394 amino acids with a calculated molecular size of 45,100. The predicted amino acid sequence contained all of the internal peptide fragment sequences derived from the purified 42 kDa enzyme. When the open reading frame was introduced into pGEX-2T vector and transfected into E. coli cells, a significant choline/ethanolamine kinase activity did appear in the cell lysate. A homology comparison with the previously reported choline kinase cDNAs (CKR1 and CKR2) from rat liver showed 66%-68% in entire nucleotide sequences and 57%-59% in amino acid sequences, indicating that the cloned cDNA here must be a novel CK/EK gene product.
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U2 - 10.1016/S0005-2760(97)00177-X
DO - 10.1016/S0005-2760(97)00177-X
M3 - Article
C2 - 9487136
AN - SCOPUS:0032484998
SN - 0005-2760
VL - 1390
SP - 1
EP - 7
JO - Biochimica et Biophysica Acta (BBA)/Lipids and Lipid Metabolism
JF - Biochimica et Biophysica Acta (BBA)/Lipids and Lipid Metabolism
IS - 1
ER -