Riise H M, Berg T, Nilssen O, Romeo G, Tollersrud O K, Ceccherini I
Department of Medical Biochemistry, Institute of Medical Biology, University of Tromsø, Norway.
Genomics. 1997 Jun 1;42(2):200-7. doi: 10.1006/geno.1997.4668.
Lysosomal alpha-mannosidase (LAMAN) (EC 3.2.1.24) is an exoglycosidase involved in the ordered degradation of N-linked oligosaccharides. Lack of LAMAN activity leads to the lysosomal storage disorder alpha-mannosidosis (MIM No. 248500). We determined the genomic organization of the human lysosomal alpha-mannosidase gene (laman; HGMW-approved symbol MANB) by using oligonucleotide primers designed from the human laman cDNA sequence as part of a PCR-based strategy. The gene spanned 21.5 kb and contained 24 exons. By primer extension analysis, the major transcription initiation sites were mapped to positions -309, -196, and -191 relative to the first in-frame ATG. No CAAT or TATA sequences could be identified within 134 bp upstream of the transcription initiation sites, but the 5' flanking region contained several GC-rich regions with putative binding sites for the transcription factors SP-1, AP-2, and ETF.
溶酶体α-甘露糖苷酶(LAMAN)(EC 3.2.1.24)是一种参与N-连接寡糖有序降解的外切糖苷酶。缺乏LAMAN活性会导致溶酶体贮积症α-甘露糖苷贮积症(MIM编号248500)。我们通过使用从人laman cDNA序列设计的寡核苷酸引物,作为基于PCR策略的一部分,确定了人溶酶体α-甘露糖苷酶基因(laman;HGMW批准符号MANB)的基因组结构。该基因跨度为21.5 kb,包含24个外显子。通过引物延伸分析,主要转录起始位点被定位到相对于第一个读码框ATG的-309、-196和-191位置。在转录起始位点上游134 bp内未发现CAAT或TATA序列,但5'侧翼区域包含几个富含GC的区域,具有转录因子SP-1、AP-2和ETF的假定结合位点。