Molecular Cell Biology Program, Washington University, St Louis, MO 63110, USA.
Dis Model Mech. 2010 Jul-Aug;3(7-8):407-14. doi: 10.1242/dmm.001701.
The high rate of preterm birth in the USA and many other countries is a potential target for improving children's immediate health and reducing the medical problems they face as adults. The acute complications for infants born prematurely often require intensive care management and are followed by long-lasting cognitive, sensory, motor, and cardiovascular deficits that substantially limit adult capabilities and survival. The inability to effectively reduce preterm birth stems from the failure to understand normal mechanisms of parturition in humans. Although studies from several model organisms help define the physiology of maintenance and termination of pregnancy, there are fundamental differences between species. For example, species regulate their production of progesterone, the crucial hormone in sustaining pregnancy, differently. This limits the extent to which models can provide meaningful information about the physiological mechanisms of human gestation. The growing wealth of sequenced mammalian genomes, computational comparative genomic tools and systems biology approaches provides new potential to utilize the divergence of DNA sequences and physiology between species to understand the genetic underpinnings of preterm birth.
美国和许多其他国家早产率高,这是改善儿童即时健康和减少他们成年后面临的医疗问题的一个潜在目标。早产儿出生时的急性并发症通常需要重症监护管理,随后会出现长期的认知、感觉、运动和心血管缺陷,这大大限制了成年人的能力和生存。无法有效降低早产率源于未能理解人类分娩的正常机制。尽管来自几个模式生物的研究有助于定义妊娠维持和终止的生理学,但物种之间存在根本差异。例如,物种对维持妊娠的关键激素孕酮的产生有不同的调节方式。这限制了模型在多大程度上可以提供关于人类妊娠生理机制的有意义信息。越来越多的已测序哺乳动物基因组、计算比较基因组工具和系统生物学方法为利用物种间 DNA 序列和生理学的差异来理解早产的遗传基础提供了新的潜力。