Peg5/Neuronatin is an imprinted gene located on sub-distal chromosome 2 in the mouse

被引:86
作者
Kagitani, F
Kuroiwa, Y
Wakana, S
Shiroishi, T
Miyoshi, N
Kobayashi, S
Nishida, M
Kohda, T
KanekoIshino, T
Ishino, F
机构
[1] TOKYO INST TECHNOL,CTR GENE RES,MIDORI KU,YOKOHAMA,KANAGAWA 226,JAPAN
[2] CENT INST EXPT ANIM,MIYAMAE KU,KAWASAKI,KANAGAWA 216,JAPAN
[3] NATL INST GENET,DEPT MAMMALIAN GENET,SHIZUOKA 411,JAPAN
[4] TOKAI UNIV,SCH HLTH SCI,ISEHARA,KANAGAWA 25911,JAPAN
[5] JAPAN SCI & TECHNOL CORP,PRESTO,JST,KAWAGUCHI,SAITAMA 332,JAPAN
基金
日本科学技术振兴机构;
关键词
D O I
10.1093/nar/25.17.3428
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have established a systematic screen for imprinted genes using a subtraction-hybridization method with day 8.5 fertilized and parthenogenetic embryos, Two novel imprinted genes, Peg1/Mest and Peg3, were identified previously by this method, along with the two known imprinted genes, lgf2 and Snrpn. Recently three additional candidate imprinted genes, Peg5-7, were detected and Peg5 is analyzed further in this study, The cDNA sequence of Peg5 is identical to Neuronatin, a gene recently reported to be expressed mainly in the brain, Two novel spliced forms were detected with some additional sequence in the middle of the known Neuronatin sequences. All alternatively spliced forms of Peg5 were expressed only from the paternal allele, confirmed using DNA polymorphism in a subinterspecific cross. Peg5/Neuronatin maps to sub-distal Chr 2, proximal to the previously established imprinted region where imprinted genes cause abnormal shape and behavior in neonates.
引用
收藏
页码:3428 / 3432
页数:5
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