Buetow K H, Shiang R, Yang P, Nakamura Y, Lathrop G M, White R, Wasmuth J J, Wood S, Berdahl L D, Leysens N J
Division of Population Science, Fox Chase Cancer Center, Philadelphia, PA 19111.
Am J Hum Genet. 1991 May;48(5):911-25.
Utilizing the CEPH reference panel and genotypic data for 53 markers, we have constructed a 20-locus multipoint genetic map of human chromosome 4. New RFLPs are reported for four loci. The map integrates a high-resolution genetic map of 4p16 into a continuous map extending to 4q31 and an unlinked cluster of three loci at 4q35. The 20 linked markers form a continuous linkage group of 152 cM in males and 202 cM in females. Likely genetic locations are provided for 25 polymorphic anonymous sequences and 28 gene-specific RFLPs. The map was constructed employing the LINKAGE and CRIMAP computational methodologies to build the multipoint map via a stepwise algorithm. A detailed 10-point map of the 4p16 region constructed from the CEPH panel provides evidence for heterogeneity in the linkage maps constructed from families segregating for Huntington disease (HD). It additionally provides evidence for position-specific recombination frequencies in the telomeric region of 4p.
利用CEPH参考面板和53个标记的基因型数据,我们构建了人类4号染色体的一个包含20个位点的多点遗传图谱。报道了四个位点的新限制性片段长度多态性(RFLP)。该图谱将4p16的高分辨率遗传图谱整合到一个延伸至4q31的连续图谱以及4q35处三个位点的一个不连锁簇中。这20个连锁标记在男性中形成一个152厘摩(cM)的连续连锁群,在女性中形成一个202 cM的连续连锁群。为25个多态性匿名序列和28个基因特异性RFLP提供了可能的遗传定位。该图谱是通过使用LINKAGE和CRIMAP计算方法,经由逐步算法构建多点图谱而构建的。从CEPH面板构建的4p16区域的详细十点图谱为从亨廷顿舞蹈病(HD)家系构建的连锁图谱中的异质性提供了证据。它还为4p端粒区域中位置特异性重组频率提供了证据。