TY - JOUR
T1 - Myelin proteolipid protein gene structure and its regulation of expression in normal and jimpy mutant mice
AU - Ikenaka, Kazuhiro
AU - Furuichi, Teiichi
AU - Iwasaki, Yasuno
AU - Moriguchi, Akira
AU - Okano, Hideyuki
AU - Mikoshiba, Katsuhiko
N1 - Funding Information:
This study was performed with the aid of Special Co-ordination Funds from the Science and Technology Agency of the Japanese Government. This study was also supported by a grant from the National Center for Nervous, Mental and Muscular Disorders of the Ministry of Health and Welfare, and a Grant-in-Aid for Scientific Research from the Ministry of Education, Japan. The authors thank Dr J. Gregor Sutcliffe for providing us with the rat PLP-cDPU’A clone, ~27, and Dr Kazunori Shimada for providing the mouse genomic library for use in our study. We also thank Mr Kunitatsu Izumi for synthesizing the oligonucleotides and Mr Tetsushi Kagawa for his technical assistance.
PY - 1988/2/20
Y1 - 1988/2/20
N2 - The mouse proteolipid protein (PLP) gene was cloned into the λ bacteriophage Charon 4A. The organization and the nucleotide sequence of the exons of the mouse PLP gene were quite similar to those of their human counterparts, consisting of seven exons. The transcription of the PLP gene started from multiple sites. There was a unique sequence tandemly repeated four times, sharing homology with the herpes simplex virus DR2 sequence, upstream from the transcribed region. Expression of the myelin basic protein (MBP) is also restricted to the oligodendrocytes in the central nervous system as is the PLP expression. Homology search against the mouse MBP gene revealed that several boxes in the 5′-flanking region of PLP show a high degree of homology with the sequence present in the MBP 5′-flanking region, possibly of importance in the concomitant expression of both genes in the central nervous system. PLP-mRNA in jimpy mutant mice does not contain exon 5 and its content is greatly reduced. We analyzed the jimpy PLP-mRNA and showed that the transcription initiated from the same sites as those in normal mice. Cloning and sequencing of the 5′-flanking region of the jimpy PLP gene revealed that there were no mutations in the promoter region of the jimpy PLP gene. Therefore, it is likely that a mutation, presumably existing within the jimpy PLP gene, caused the skipping of exon 5 and directly affected the mRNA level.
AB - The mouse proteolipid protein (PLP) gene was cloned into the λ bacteriophage Charon 4A. The organization and the nucleotide sequence of the exons of the mouse PLP gene were quite similar to those of their human counterparts, consisting of seven exons. The transcription of the PLP gene started from multiple sites. There was a unique sequence tandemly repeated four times, sharing homology with the herpes simplex virus DR2 sequence, upstream from the transcribed region. Expression of the myelin basic protein (MBP) is also restricted to the oligodendrocytes in the central nervous system as is the PLP expression. Homology search against the mouse MBP gene revealed that several boxes in the 5′-flanking region of PLP show a high degree of homology with the sequence present in the MBP 5′-flanking region, possibly of importance in the concomitant expression of both genes in the central nervous system. PLP-mRNA in jimpy mutant mice does not contain exon 5 and its content is greatly reduced. We analyzed the jimpy PLP-mRNA and showed that the transcription initiated from the same sites as those in normal mice. Cloning and sequencing of the 5′-flanking region of the jimpy PLP gene revealed that there were no mutations in the promoter region of the jimpy PLP gene. Therefore, it is likely that a mutation, presumably existing within the jimpy PLP gene, caused the skipping of exon 5 and directly affected the mRNA level.
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U2 - 10.1016/0022-2836(88)90303-8
DO - 10.1016/0022-2836(88)90303-8
M3 - Article
C2 - 2451027
AN - SCOPUS:0023942004
SN - 0022-2836
VL - 199
SP - 587
EP - 596
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 4
ER -