Bugge M, Bruun-Petersen G, Brøndum-Nielsen K, Friedrich U, Hansen J, Jensen G, Jensen P K, Kristoffersson U, Lundsteen C, Niebuhr E, Rasmussen K R, Rasmussen K, Tommerup N
Department of Medical Genetics, IMBG, University of Copenhagen, Blegdamsvej 3, DK-2200 Copenhagen N, Denmark.
J Med Genet. 2000 Nov;37(11):858-65. doi: 10.1136/jmg.37.11.858.
Disease associated balanced chromosomal rearrangements (DBCRs), which truncate, delete, or otherwise inactivate specific genes, have been instrumental for positional cloning of many disease genes. A network of cytogenetic laboratories, Mendelian Cytogenetics Network (MCN), has been established to facilitate the identification and mapping of DBCRs. To get an estimate of the potential of this approach, we surveyed all cytogenetic archives in Denmark and southern Sweden, with a population of approximately 6.6 million. The nine laboratories have performed 71 739 postnatal cytogenetic tests. Excluding Robertsonian translocations and chromosome 9 inversions, we identified 216 DBCRs ( approximately 0.3%), including a minimum estimate of 114 de novo reciprocal translocations (0.16%) and eight de novo inversions (0.01%). Altogether, this is six times more frequent than in the general population, suggesting a causal relationship with the traits involved in most of these cases. Of the identified cases, only 25 (12%) have been published, including 12 cases with known syndromes and 13 cases with unspecified mental retardation/congenital malformations. The remaining DBCRs were associated with a plethora of traits including mental retardation, dysmorphic features, major congenital malformations, autism, and male and female infertility. Several of the unpublished DBCRs defined candidate breakpoints for nail-patella, Prader-Willi, and Schmidt syndromes, ataxia, and ulna aplasia. The implication of the survey is apparent when compared with MCN; altogether, the 292 participating laboratories have performed >2.5 million postnatal analyses, with an estimated approximately 7500 DBCRs stored in their archives, of which more than half might be causative mutations. In addition, an estimated 450-500 novel cases should be detected each year. Our data illustrate that DBCRs and MCN are resources for large scale establishment of phenotype-genotype relationships in man.
与疾病相关的平衡染色体重排(DBCRs)会截断、删除或以其他方式使特定基因失活,对许多疾病基因的定位克隆起到了重要作用。一个细胞遗传学实验室网络,即孟德尔细胞遗传学网络(MCN)已经建立,以促进DBCRs的识别和定位。为了评估这种方法的潜力,我们调查了丹麦和瑞典南部所有的细胞遗传学档案,该地区人口约为660万。这九个实验室共进行了71739次产后细胞遗传学检测。排除罗伯逊易位和9号染色体倒位,我们鉴定出216个DBCRs(约0.3%),其中至少估计有114个新发相互易位(0.16%)和8个新发倒位(0.01%)。总体而言,这比普通人群中的频率高六倍,表明与大多数这些病例所涉及的性状存在因果关系。在已鉴定的病例中,只有25例(12%)已发表,包括12例已知综合征病例和13例未明确的智力发育迟缓/先天性畸形病例。其余的DBCRs与多种性状相关,包括智力发育迟缓、畸形特征、主要先天性畸形、自闭症以及男性和女性不育。一些未发表的DBCRs确定了指甲-髌骨综合征、普拉德-威利综合征、施密特综合征、共济失调和尺骨发育不全的候选断点。与MCN相比,该调查的意义显而易见;总共有292个参与实验室进行了超过250万次产后分析,估计其档案中存储了约7500个DBCRs,其中一半以上可能是致病突变。此外,估计每年应检测到450 - 500个新病例。我们的数据表明,DBCRs和MCN是大规模建立人类表型-基因型关系的资源。