Naylor S L, Marshall A, Hensel C, Martinez P F, Holley B, Sakaguchi A Y
Department of Cellular and Structural Biology, University of Texas Health Science Center, San Antonio 78284.
Genomics. 1989 Apr;4(3):355-61. doi: 10.1016/0888-7543(89)90342-x.
Small cell lung cancer (SCLC) has been associated with a deletion of the short arm of chromosome 3. One SCLC cell line, H748, has an interstitial deletion of chromosome 3p and shows allele loss for the DNF15S2 locus detected by the probe lambda H3. Conservation of DNF15S2 sequences in mouse indicated that this human genomic fragment may contain coding sequences. Screening of a normal lung cDNA library with chromosome 3-specific fragments of the lambda H3 probe resulted in the isolation of 18 positive clones. The cDNA clones detect an additional DNA polymorphism that is in linkage disequilibrium with the HindIII polymorphism of the DNF15S2 locus. Sequence analysis indicated that the DNF15S2 locus could potentially code for a previously unreported protein of 67 kDa which has 26 cysteine residues. DNF15S2 is part of the coding region of a 3.3-kb mRNA expressed in lung. Northern analysis indicated that this mRNA was not detectable in one of five SCLC lines. This SCLC line, H128, also lacks the enzyme aminoacylase 1.
小细胞肺癌(SCLC)与3号染色体短臂缺失有关。一种小细胞肺癌细胞系H748,存在3号染色体短臂的中间缺失,并显示出用探针λH3检测到的DNF15S2基因座的等位基因缺失。DNF15S2序列在小鼠中的保守性表明该人类基因组片段可能包含编码序列。用λH3探针的3号染色体特异性片段筛选正常肺cDNA文库,得到18个阳性克隆。这些cDNA克隆检测到另一种DNA多态性,该多态性与DNF15S2基因座的HindIII多态性处于连锁不平衡状态。序列分析表明,DNF