A novel pleckstrin homology-related gene family defined by Ipl/Tssc3, TDAG51, and Tih1:: tissue-specific expression, chromosomal location, and parental imprinting

被引:88
作者
Frank, D
Mendelsohn, CL
Ciccone, E
Svensson, K
Ohlsson, R
Tycko, B
机构
[1] Columbia Univ Coll Phys & Surg, Inst Canc Genet, New York, NY 10032 USA
[2] Columbia Univ Coll Phys & Surg, Dept Pathol, New York, NY 10032 USA
[3] Columbia Univ Coll Phys & Surg, Dept Urol, New York, NY 10032 USA
[4] Columbia Univ Coll Phys & Surg, Dept Pathol, New York, NY 10032 USA
[5] Univ Uppsala, Dept Genet & Anim Dev, Uppsala, Sweden
关键词
D O I
10.1007/s003359901182
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 previously described a gene, Ipi (Tssc3), that is expressed selectively from the maternal allele in placenta, yolk sac, and fetal liver and that maps within the imprinted domain of mouse distal Chromosome (Chr) 7/human Chr 11p15.5 (Hum Mol Genet 6, 2021, 1997). Ipl is similar to TDAG51, a gene that is involved in FAS/CD95 expression. Here we describe another gene, Tihl (TDAG/Ipl homologue 1), with equivalent sequence similarity to Ipl. Structural prediction indicates that the products of these three genes share a central motif resembling a pleckstrin-homology (PH) domain, and TIH1 protein has weal; sequence similarity to the PH-domain protein SEC7/CYTOHESIN. Like Ipl, Tihl is a small gene with a single small intron. Tih1 maps to distal mouse Chr 1 and human Chr 1q31, chromosomal regions that have not shown evidence for imprinting and, in contrast to Ipl, Tih1 is expressed equally from both parental alleles. Ipl, Tih1, and TDAG51 have overlapping but distinct patterns of expression. Tih1 and TDAG51 are expressed in multiple fetal and adult tissues. In contrast, during early mouse development Ipl mRNA and protein are highly specific for two tissues involved in maternal/fetal exchange: visceral endoderm of the yolk sac and labyrinthine trophoblast of the placenta. These findings highlight the dominance of chromosomal contest over gene structure in some examples of parental imprinting and extend previous evidence for placenta-specific expression of imprinted genes. The data also define a new subfamily of PH domain genes.
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页码:1150 / 1159
页数:10
相关论文
共 37 条
[11]   GENOMIC IMPRINTING OF MASH2, A MOUSE GENE REQUIRED FOR TROPHOBLAST DEVELOPMENT [J].
GUILLEMOT, F ;
CASPARY, T ;
TILGHMAN, SM ;
COPELAND, NG ;
GILBERT, DJ ;
JENKINS, NA ;
ANDERSON, DJ ;
JOYNER, AL ;
ROSSANT, J ;
NAGY, A .
NATURE GENETICS, 1995, 9 (03) :235-242
[12]   Parental antagonism, relatedness asymmetries, and genomic imprinting [J].
Haig, D .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1997, 264 (1388) :1657-1662
[13]  
HAIG D, 1991, CELL, V64, P1045
[14]  
HEDBORG F, 1994, AM J PATHOL, V145, P802
[15]   Imprinted genes have few and small introns [J].
Hurst, LD ;
McVean, G ;
Moore, T .
NATURE GENETICS, 1996, 12 (03) :234-237
[16]   Growth effects of uniparental disomies and the conflict theory of genomic imprinting [J].
Hurst, LD ;
McVean, GT .
TRENDS IN GENETICS, 1997, 13 (11) :436-443
[17]   alpha L beta 2 integrin/LFA-1 binding to ICAM-1 induced by cytohesin-1, a cytoplasmic regulatory molecule [J].
Kolanus, W ;
Nagel, W ;
Schiller, B ;
Zeitlmann, L ;
Godar, S ;
Stockinger, H ;
Seed, B .
CELL, 1996, 86 (02) :233-242
[18]   Interpreting cDNA sequences: Some insights from studies on translation [J].
Kozak, M .
MAMMALIAN GENOME, 1996, 7 (08) :563-574
[19]   CLONING OR P57(KIP2), A CYCLIN-DEPENDENT KINASE INHIBITOR WITH UNIQUE DOMAIN-STRUCTURE AND TISSUE DISTRIBUTION [J].
LEE, MH ;
REYNISDOTTIR, I ;
MASSAGUE, J .
GENES & DEVELOPMENT, 1995, 9 (06) :639-649
[20]  
Lee MP, 1998, CANCER RES, V58, P1052