Higgins Anne W, Alkuraya Fowzan S, Bosco Amy F, Brown Kerry K, Bruns Gail A P, Donovan Diana J, Eisenman Robert, Fan Yanli, Farra Chantal G, Ferguson Heather L, Gusella James F, Harris David J, Herrick Steven R, Kelly Chantal, Kim Hyung-Goo, Kishikawa Shotaro, Korf Bruce R, Kulkarni Shashikant, Lally Eric, Leach Natalia T, Lemyre Emma, Lewis Janine, Ligon Azra H, Lu Weining, Maas Richard L, MacDonald Marcy E, Moore Steven D P, Peters Roxanna E, Quade Bradley J, Quintero-Rivera Fabiola, Saadi Irfan, Shen Yiping, Shendure Jay, Williamson Robin E, Morton Cynthia C
Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
Am J Hum Genet. 2008 Mar;82(3):712-22. doi: 10.1016/j.ajhg.2008.01.011.
Apparently balanced chromosomal rearrangements in individuals with major congenital anomalies represent natural experiments of gene disruption and dysregulation. These individuals can be studied to identify novel genes critical in human development and to annotate further the function of known genes. Identification and characterization of these genes is the goal of the Developmental Genome Anatomy Project (DGAP). DGAP is a multidisciplinary effort that leverages the recent advances resulting from the Human Genome Project to increase our understanding of birth defects and the process of human development. Clinically significant phenotypes of individuals enrolled in DGAP are varied and, in most cases, involve multiple organ systems. Study of these individuals' chromosomal rearrangements has resulted in the mapping of 77 breakpoints from 40 chromosomal rearrangements by FISH with BACs and fosmids, array CGH, Southern-blot hybridization, MLPA, RT-PCR, and suppression PCR. Eighteen chromosomal breakpoints have been cloned and sequenced. Unsuspected genomic imbalances and cryptic rearrangements were detected, but less frequently than has been reported previously. Chromosomal rearrangements, both balanced and unbalanced, in individuals with multiple congenital anomalies continue to be a valuable resource for gene discovery and annotation.
患有严重先天性异常个体中的明显平衡染色体重排代表了基因破坏和失调的自然实验。可以对这些个体进行研究,以鉴定对人类发育至关重要的新基因,并进一步阐明已知基因的功能。鉴定和表征这些基因是发育基因组解剖计划(DGAP)的目标。DGAP是一项多学科的工作,它利用了人类基因组计划带来的最新进展,以增进我们对出生缺陷和人类发育过程的理解。参与DGAP的个体具有临床意义的表型各不相同,并且在大多数情况下,涉及多个器官系统。对这些个体染色体重排的研究已通过使用BAC和fosmid的FISH、阵列CGH、Southern印迹杂交、MLPA、RT-PCR和抑制PCR,对40个染色体重排中的77个断点进行了定位。18个染色体断点已被克隆和测序。检测到了意想不到的基因组失衡和隐匿重排,但频率低于先前报道。患有多种先天性异常个体中的染色体重排,无论是平衡的还是不平衡的,仍然是基因发现和注释的宝贵资源。