Harris P, Lalande M, Stroh H, Bruns G, Flint A, Latt S A
Mental Retardation Center, Children's Hospital, Boston, MA 02115.
Hum Genet. 1987 Oct;77(2):95-103. doi: 10.1007/BF00272372.
A flow sorted chromosome 16-enriched recombinant library was produced to isolate DNA probes useful for constructing a linkage map of 16p, primarily for the study of adult polycystic kidney disease (APKD). The APKD locus has been mapped to chromosome 16 by linkage with the probe 3'HVR, which is located in the region 16p12----pter. Of the 48 single-copy fragments isolated from this new phage library, 39 (81%) were found to be chromosome 16 specific. Probes mapping to chromosome 16 were regionally localized by hybridizing to flow-sorted spot blots of translocation products from lymphoblastoid cell lines containing the rearrangements t(1;16) or t(11;16). Translocation breakpoints at 16p13.11 and 16p11.1 were utilized to subdivide chromosome 16 into three regions: Twenty-six probes were mapped to 16p11.1----16qter, two to 16p11.1----16p13.11, and eleven to 16p13.11----16pter. Probes from 16p were examined for their recognition of restriction fragment length polymorphisms (RFLPs). Seven polymorphic probes were found which recognized eleven RFLPs. Six of the seven probes have RFLPs which are reasonably informative (polymorphism information contents (PIC) of over 0.25). Two of these identify polymorphisms with three different alleles, one of which has a PIC value of over 0.4. These probes may aid in the diagnosis of APKD and contribute towards a linkage map of chromosome 16.
构建了一个经流式细胞仪分选的富含16号染色体的重组文库,以分离对构建16p连锁图谱有用的DNA探针,主要用于成人多囊肾病(APKD)的研究。APKD基因座已通过与位于16p12----pter区域的探针3'HVR连锁而定位到16号染色体上。从这个新的噬菌体文库中分离出的48个单拷贝片段中,有39个(81%)被发现是16号染色体特异性的。通过与含有t(1;16)或t(11;16)重排的淋巴母细胞系的易位产物的流式细胞仪分选斑点杂交,将定位到16号染色体的探针进行区域定位。利用16p13.11和16p11.1处的易位断点将16号染色体分为三个区域:26个探针定位到16p11.1----16qter,2个定位到16p11.1----16p13.11,11个定位到16p13.11----16pter。检测了来自16p的探针识别限制性片段长度多态性(RFLP)的能力。发现了7个多态性探针,它们识别11个RFLP。7个探针中的6个具有信息丰富的RFLP(多态性信息含量(PIC)超过0.25)。其中2个探针鉴定出具有三个不同等位基因的多态性,其中一个的PIC值超过0.4。这些探针可能有助于APKD的诊断,并有助于构建16号染色体的连锁图谱。