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肝富集基因 1a 和 1b 编码新型分泌蛋白,对斑马鱼正常肝脏发育至关重要。

liver-enriched gene 1a and 1b encode novel secretory proteins essential for normal liver development in zebrafish.

机构信息

College of Animal Sciences, Zhejiang University, Hangzhou, People's Republic of China.

出版信息

PLoS One. 2011;6(8):e22910. doi: 10.1371/journal.pone.0022910. Epub 2011 Aug 9.

Abstract

liver-enriched gene 1 (leg1) is a liver-enriched gene in zebrafish and encodes a novel protein. Our preliminary data suggested that Leg1 is probably involved in early liver development. However, no detailed characterization of Leg1 has been reported thus far. We undertook both bioinformatic and experimental approaches to study leg1 gene structure and its role in early liver development. We found that Leg1 identifies a new conserved protein superfamily featured by the presence of domain of unknown function 781 (DUF781). There are two copies of leg1 in zebrafish, namely leg1a and leg1b. Both leg1a and leg1b are expressed in the larvae and adult liver with leg1a being the predominant form. Knockdown of Leg1a or Leg1b by their respective morpholinos specifically targeting their 5'-UTR each resulted in a small liver phenotype, demonstrating that both Leg1a and Leg1b are important for early liver development. Meanwhile, we found that injection of leg1-ATG(MO), a morpholino which can simultaneously block the translation of Leg1a and Leg1b, caused not only a small liver phenotype but hypoplastic exocrine pancreas and intestinal tube as well. Further examination of leg1-ATG(MO) morphants with early endoderm markers and early hepatic markers revealed that although depletion of total Leg1 does not alter the hepatic and pancreatic fate of the endoderm cells, it leads to cell cycle arrest that results in growth retardation of liver, exocrine pancreas and intestine. Finally, we proved that Leg1 is a secretory protein. This intrigued us to propose that Leg1 might act as a novel secreted regulator that is essential for liver and other digestive organ development in zebrafish.

摘要

肝富集基因 1(leg1)是斑马鱼肝脏富集基因,编码一种新型蛋白。我们的初步数据表明 Leg1 可能参与早期肝脏发育。然而,迄今为止尚未报道其详细特征。我们采用生物信息学和实验方法研究 leg1 基因结构及其在早期肝脏发育中的作用。我们发现 Leg1 确定了一个新的保守蛋白超家族,其特征是存在未知功能域 781(DUF781)。在斑马鱼中有两个 leg1 拷贝,即 leg1a 和 leg1b。leg1a 和 leg1b 在幼虫和成年肝脏中均有表达,且 leg1a 为主要形式。通过针对其 5'UTR 的各自 morpholino 特异性敲低 Leg1a 或 Leg1b,导致肝脏变小表型,表明 Leg1a 和 Leg1b 均对早期肝脏发育至关重要。同时,我们发现注射 leg1-ATG(MO),一种可同时阻断 Leg1a 和 Leg1b 翻译的 morpholino,不仅导致肝脏变小表型,还导致外分泌胰腺和肠管发育不良。进一步检查 leg1-ATG(MO)嵌合体的早期内胚层标记物和早期肝标记物表明,尽管耗尽总 Leg1 不会改变内胚层细胞的肝和胰腺命运,但它会导致细胞周期停滞,从而导致肝脏、外分泌胰腺和肠道生长迟缓。最后,我们证明 Leg1 是一种分泌蛋白。这引起了我们的兴趣,提出 Leg1 可能作为一种新型分泌调节剂,对于斑马鱼肝脏和其他消化器官的发育是必不可少的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d577/3153479/7d075787ab18/pone.0022910.g001.jpg

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