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LIN28介导的基因调控环在整个器官发生过程中同步转变。

LIN28-mediated gene regulatory loops synchronize transitions throughout organogenesis.

作者信息

Thevarajan Indhujah, Osuna Maria F, Lewey Sonia Fuentes, Sauceda Eustolia, Briseno Sayra, Griffin Caylah, Kim Bareun, Rowe R Grant, da Rocha Edroaldo Lummertz, Osborne Jihan K

机构信息

Department of Pharmacology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX, 75390, USA.

Division of Pediatric Hematology/Oncology, Boston Children's Hospital, Boston, MA, 02115, USA.

出版信息

Biochem Biophys Rep. 2025 Sep 16;44:102226. doi: 10.1016/j.bbrep.2025.102226. eCollection 2025 Dec.

DOI:10.1016/j.bbrep.2025.102226
PMID:41019289
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12465051/
Abstract

Control of the intervals between proliferation and differentiation of stem/progenitor cells is coordinated by developmental regulators, comprised of both microRNAs (miRNAs) and proteins, termed heterochronic genes. The heterochronic factors, Lin28-RNA-binding proteins (RBPs) and the miRNAs- comprise a unique subset of evolutionarily conserved genes that regulate the developmental timing of metazoans, from worms to mammals. While there has been much investigation into the reciprocal negative feedback loop between LIN-28 and during fetal development and cancer. Few have investigated how positive regulatory loops between the mammalian Lin28-RBPs, and mRNAs order spatiotemporal transitions of progenitors from specification to organogenesis. Screening for factors that activated luciferase reporters of the human and promoters, in combination with genetic mouse models, we demonstrate positive feedforward loops between key developmental transcription factors such as B-Catenin, Sox2, Sox9, and Lin28-RBPs. Furthermore, we demonstrate heterochronic regulation of morphogenesis is not only genetically modulated but also molecularly fine-tuned via position-dependent sequences in the 5' and/or 3' untranslated regions.

摘要

干细胞/祖细胞增殖与分化之间的时间间隔由发育调节因子协调控制,这些调节因子包括微小RNA(miRNA)和蛋白质,即异时性基因。异时性因子、Lin28-RNA结合蛋白(RBP)和miRNA构成了一个独特的进化保守基因子集,从蠕虫到哺乳动物,它们调节后生动物的发育时间。虽然在胎儿发育和癌症期间,人们对LIN-28和之间的相互负反馈环进行了大量研究。但很少有人研究哺乳动物Lin28-RBP和mRNA之间的正调节环如何调控祖细胞从特化到器官发生的时空转变。通过筛选激活人类和启动子荧光素酶报告基因的因子,并结合基因小鼠模型,我们证明了关键发育转录因子如β-连环蛋白、Sox2、Sox9和Lin28-RBP之间存在正前馈环。此外,我们证明形态发生的异时性调节不仅受到基因调控,还通过5'和/或3'非翻译区中位置依赖序列进行分子微调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/34a9a6f1e505/mmcfigs5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/298de82354e9/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/03849e6333df/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/80fe59de5a25/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/f68d2980925d/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/61acab4fe59d/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/4a4519563818/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/d11d6a8d35e9/mmcfigs1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/064cec744601/mmcfigs2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/a364ee2ab3b5/mmcfigs3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/4fe586dad311/mmcfigs4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/34a9a6f1e505/mmcfigs5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/298de82354e9/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/03849e6333df/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/80fe59de5a25/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/f68d2980925d/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/61acab4fe59d/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/4a4519563818/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/d11d6a8d35e9/mmcfigs1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/064cec744601/mmcfigs2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/a364ee2ab3b5/mmcfigs3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/4fe586dad311/mmcfigs4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5349/12465051/34a9a6f1e505/mmcfigs5.jpg

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