Marker P C, King J A, Copeland N G, Jenkins N A, Kingsley D M
Department of Developmental Biology, Beckman Center, Stanford University School of Medicine, California 94305-5427, USA.
Genomics. 1995 Aug 10;28(3):576-80. doi: 10.1006/geno.1995.1192.
Murine Bmp7 has been assigned to distal Chromosome 2 by interspecific backcross mapping. The map location suggests close linkage to classical mouse mutations and places Bmp7 within a chromosome region thought to contain one or more unidentified imprinted genes. A direct test suggests that Bmp7 is not imprinted. An examination of embryonic RNA expression patterns shows that Bmp7 is expressed in a variety of skeletal and nonskeletal tissues. Both embryonic expression patterns and the human chromosomal sublocalization inferred from its mouse location make Bmp7 a candidate for the gene affected in some patients with Holt-Oram syndrome.
通过种间回交定位,小鼠Bmp7基因被定位到2号染色体远端。该图谱位置表明它与经典的小鼠突变紧密连锁,并将Bmp7置于一个被认为包含一个或多个未鉴定的印记基因的染色体区域内。直接检测表明Bmp7不是印记基因。对胚胎RNA表达模式的检查显示,Bmp7在多种骨骼和非骨骼组织中表达。胚胎表达模式以及根据其在小鼠中的位置推断出的人类染色体亚定位,都使Bmp7成为一些患有心脏手综合征患者中受影响基因的候选基因。