HOX11L1, a gene involved in peripheral nervous system development, maps to human chromosome 2p13.1→p12 and mouse chromosome 6C3-D1

被引:9
作者
Puliti, A
Cinti, R
Betsos, N
Romeo, G
Ceccherini, I
机构
[1] Ist Giannina Gaslini, Genet Mol Lab, I-16148 Genoa, Italy
[2] Univ Pisa, Dipartimento Sci Uomo & Ambiente, I-56100 Pisa, Italy
[3] IARC, Genet Canc Susceptibil Unit, Lyon, France
[4] Univ Genoa, Dipartimento Oncol Biol & Genet, I-16126 Genoa, Italy
来源
CYTOGENETICS AND CELL GENETICS | 1999年 / 84卷 / 1-2期
关键词
D O I
10.1159/000015234
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
HOX11L1 is a homeobox gene involved in peripheral nervous system development as confirmed by knockout mice exhibiting megacolon with enteric ganglia, a phenotype associated in human with Intestinal Neuronal Dysplasia (IND). Using FISH and radiation hybrids we have localized HOX11L1 to human chromosome 2p13.1 --> p12, in a 14-cR interval between WI-5987 (D2S2088) and GCT1B4 (D2S2497), and confirmed the synteny between mouse 6C3D1 and human 2p13.1 --> p12 chromosomes by mapping an EST cDNA clone corresponding to mouse HOX 11L1 (Tlx2).
引用
收藏
页码:115 / 117
页数:3
相关论文
共 13 条
[1]  
Barone V, 1996, AM J MED GENET, V62, P195, DOI 10.1002/(SICI)1096-8628(19960315)62:2<195::AID-AJMG15>3.0.CO
[2]  
2-J
[3]   THE HOX11 GENE ENCODES A DNA-BINDING NUCLEAR TRANSCRIPTION FACTOR BELONGING TO A DISTINCT FAMILY OF HOMEOBOX GENES [J].
DEAR, TN ;
SANCHEZGARCIA, I ;
RABBITTS, TH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (10) :4431-4435
[4]   A comprehensive genetic map of the human genome based on 5,264 microsatellites [J].
Dib, C ;
Faure, S ;
Fizames, C ;
Samson, D ;
Drouot, N ;
Vignal, A ;
Millasseau, P ;
Marc, S ;
Hazan, J ;
Seboun, E ;
Lathrop, M ;
Gyapay, G ;
Morissette, J ;
Weissenbach, J .
NATURE, 1996, 380 (6570) :152-154
[5]   Ncx, a Hox11 related gene, is expressed in a variety of tissues derived from neural crest cells [J].
Hatano, M ;
Iitsuka, Y ;
Yamamoto, H ;
Dezawa, M ;
Yusa, S ;
Kohno, Y ;
Tokuhisa, T .
ANATOMY AND EMBRYOLOGY, 1997, 195 (05) :419-425
[6]   A novel pathogenesis of megacolon in Ncx/Hox11L.1 deficient mice [J].
Hatano, M ;
Aoki, T ;
Dezawa, M ;
Yusa, S ;
Iitsuka, Y ;
Koseki, H ;
Taniguchi, M ;
Tokuhisa, T .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (04) :795-801
[7]   Homeobox genes in embryogenesis and pathogenesis [J].
Mark, M ;
Rijli, FM ;
Chambon, P .
PEDIATRIC RESEARCH, 1997, 42 (04) :421-429
[8]   RET mutations in human disease [J].
Pasini, B ;
Ceccherini, I ;
Romeo, G .
TRENDS IN GENETICS, 1996, 12 (04) :138-144
[9]   Assignment of mouse Gfra1, the homologue of a new human HSCR candidate gene, to the telomeric region of mouse Chromosome 19 [J].
Puliti, A ;
Cinti, R ;
Seri, M ;
Ceccherini, I ;
Romeo, G .
CYTOGENETICS AND CELL GENETICS, 1997, 78 (3-4) :291-294
[10]  
SCHARLI AF, 1992, PEDIATR SURG INT, V7, P2