Molecular cloning and characterization of a gene expressed in mouse developing tongue, mDscr5 gene, a homolog of human DSCR5 (Down syndrome critical region gene 5)

被引:5
作者
Choi, DK
Suzuki, Y
Yoshimura, S
Togashi, T
Hida, M
Taylor, TD
Wang, YP
Sugano, S
Hattori, M
Sakaki, Y
机构
[1] Univ Tokyo, Inst Med Sci, Ctr Human Genome, Minato Ku, Tokyo 1088639, Japan
[2] RIKEN, Inst Phys & Chem Res, GSC, Wako, Saitama 3510106, Japan
[3] Univ Tokyo, Inst Med Sci, Dept Virol, Minato Ku, Tokyo 1088639, Japan
[4] Kyushu Univ, Grad Sch Med Sci, Dept Mol Biol, Fukuoka 8128582, Japan
关键词
D O I
10.1007/s003350010283
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
For understanding the pathogenesis of Down syndrome (DS), it is important to identify and characterize the genes on Chromosome (Chr) 21, especially those in the Down syndrome critical region (DSCR) on Chr 21q22.2. Recently we have determined 33.5 Mb (more than 99%) of DNA sequence of Chr 21 and, from these sequence data, we identified a novel gene, DSCR5 (transcript = 0.8 kb), from DSCR by combination of computational gene prediction and cDNA screening. For functional analysis of DSCR5, we identified a mouse homolog of the DSCR5 cDNA, and termed it mDscr5 (transcript length = 0.8 kb). The gene was mapped to mouse Chr 16 C3-C4, the syntenic region of human Chr 21, and encodes an amino acid of 132 residues with 90% identity to DSCR5. In situ hybridization showed that mDscr5 is predominantly expressed in the developing tongue. To our best knowledge, no other gene in DSCR is reported to be expressed in tongue, so that DSCR5 may be the first candidate to elucidate the pathophysiology of tongue malformation observed in DS.
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收藏
页码:347 / 351
页数:5
相关论文
共 27 条
[1]  
Ardran G M, 1973, Clin Radiol, V24, P359, DOI 10.1016/S0009-9260(73)80058-3
[2]   DOWNS-SYNDROME - ABNORMAL NEUROMUSCULAR-JUNCTION IN TONGUE OF TRANSGENIC MICE WITH ELEVATED LEVELS OF HUMAN CU/ZN-SUPEROXIDE DISMUTASE [J].
AVRAHAM, KB ;
SCHICKLER, M ;
SAPOZNIKOV, D ;
YAROM, R ;
GRONER, Y .
CELL, 1988, 54 (06) :823-829
[3]   Developmentally-regulated expression of mNapor encoding an apoptosis-induced ELAV-type RNA binding protein [J].
Choi, DK ;
Ito, T ;
Tsukahara, F ;
Hirai, M ;
Sakaki, Y .
GENE, 1999, 237 (01) :135-142
[4]  
Delabar Jean-Maurice, 1993, European Journal of Human Genetics, V1, P114
[5]   DOWNS-SYNDROME AND TONGUE SIZE [J].
DODD, B ;
LEAHY, J .
MEDICAL JOURNAL OF AUSTRALIA, 1984, 140 (12) :748-748
[6]  
Epstein C.J., 1995, METABOLIC MOL BASES, P749
[7]   PANCREATIC-ISLET CELLS EXPRESS A FAMILY OF INWARDLY RECTIFYING K+ CHANNEL SUBUNITS WHICH INTERACT TO FORM G-PROTEIN-ACTIVATED CHANNELS [J].
FERRER, J ;
NICHOLS, CG ;
MAKHINA, EN ;
SALKOFF, L ;
BERNSTEIN, J ;
GERHARD, D ;
WASSON, J ;
RAMANADHAM, S ;
PERMUTT, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (44) :26086-26091
[8]   A human homologue of Drosophila minibrain (MNB) is expressed in the neuronal regions affected in Down syndrome and maps to the critical region [J].
Guimera, J ;
Casas, C ;
Pucharcos, C ;
Solans, A ;
Domenech, A ;
Planas, AM ;
Ashley, J ;
Lovett, M ;
Estivill, X ;
Pritchard, MA .
HUMAN MOLECULAR GENETICS, 1996, 5 (09) :1305-1310
[9]   The DNA sequence of human chromosome 21 [J].
Hattori, M ;
Fujiyama, A ;
Taylor, TD ;
Watanabe, H ;
Yada, T ;
Park, HS ;
Toyoda, A ;
Ishii, K ;
Totoki, Y ;
Choi, DK ;
Soeda, E ;
Ohki, M ;
Takagi, T ;
Sakaki, Y ;
Taudien, S ;
Blechschmidt, K ;
Polley, A ;
Menzel, U ;
Delabar, J ;
Kumpf, K ;
Lehmann, R ;
Patterson, D ;
Reichwald, K ;
Rump, A ;
Schillhabel, M ;
Schudy, A ;
Zimmermann, W ;
Rosenthal, A ;
Kudoh, J ;
Shibuya, K ;
Kawasaki, K ;
Asakawa, S ;
Shintani, A ;
Sasaki, T ;
Nagamine, K ;
Mitsuyama, S ;
Antonarakis, SE ;
Minoshima, S ;
Shimizu, N ;
Nordsiek, G ;
Hornischer, K ;
Brandt, P ;
Scharfe, M ;
Schön, O ;
Desario, A ;
Reichelt, J ;
Kauer, G ;
Blöcker, H ;
Ramser, J ;
Beck, A .
NATURE, 2000, 405 (6784) :311-319
[10]   Assignment of human ADP ribosylation factor (ARF) genes ARF1 and ARF3 to chromosomes 1q42 and 12q13, respectively [J].
Hirai, M ;
Kusuda, J ;
Hashimoto, K .
GENOMICS, 1996, 34 (02) :263-265