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印迹剂量作为哺乳动物垂体大小的决定因素。

Imprinted dosage as a size determinant of the mammalian pituitary gland.

机构信息

Department of Medical and Molecular Genetics, Faculty of Life Sciences and Medicine, King's College London, London, United Kingdom.

Centre for Craniofacial and Regenerative Biology, Faculty of Dentistry, Oral and Craniofacial Sciences, King's College London, London, United Kingdom.

出版信息

Elife. 2023 Aug 17;12:e84092. doi: 10.7554/eLife.84092.

Abstract

Co-regulated genes of the Imprinted Gene Network are involved in the control of growth and body size, and imprinted gene dysfunction underlies human paediatric disorders involving the endocrine system. Imprinted genes are highly expressed in the pituitary gland, among them, , a paternally expressed gene whose membrane-bound and secreted protein products can regulate proliferation and differentiation of multiple stem cell populations. Dosage of circulating DLK1 has been previously implicated in the control of growth through unknown molecular mechanisms. Here we generate a series of mouse genetic models to modify levels of expression in the pituitary gland and demonstrate that the dosage of DLK1 modulates the process of stem cell commitment with lifelong impact on pituitary gland size. We establish that stem cells are a critical source of DLK1, where embryonic disruption alters proliferation in the anterior pituitary, leading to long-lasting consequences on growth hormone secretion later in life.

摘要

印迹基因网络的共调控基因参与生长和体型的控制,印迹基因功能障碍是涉及内分泌系统的人类儿科疾病的基础。印迹基因在垂体中高度表达,其中 是一个父系表达的基因,其膜结合和分泌的蛋白产物可以调节多种干细胞群体的增殖和分化。循环 DLK1 的剂量先前通过未知的分子机制被牵涉到生长的控制中。在这里,我们生成了一系列的小鼠遗传模型来修饰垂体中 的表达水平,并证明了 DLK1 的剂量调节干细胞分化的过程,对垂体大小具有终身影响。我们确定了干细胞是 DLK1 的一个关键来源,其中胚胎破坏改变了前垂体的增殖,导致生命后期生长激素分泌的长期后果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86c2/10468206/490fcddc5152/elife-84092-fig1.jpg

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