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TIP55 a splice isoform of the KAT5 acetyltransferase is essential for developmental gene regulation and organogenesis

机译:TIP55KAT5乙酰转移酶的剪接同工型对于发育基因调控和器官发生至关重要

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摘要

Regulation of chromatin structure is critical for cell type-specific gene expression. Many chromatin regulatory complexes exist in several different forms, due to alternative splicing and differential incorporation of accessory subunits. However, in vivo studies often utilize mutations that eliminate multiple forms of complexes, preventing assessment of the specific roles of each. Here we examined the developmental roles of the TIP55 isoform of the KAT5 histone acetyltransferase. In contrast to the pre-implantation lethal phenotype of mice lacking all four Kat5 transcripts, mice specifically deficient for Tip55 die around embryonic day 11.5 (E11.5). Prior to developmental arrest, defects in heart and neural tube were evident in Tip55 mutant embryos. Specification of cardiac and neural cell fates appeared normal in Tip55 mutants. However, cell division and survival were impaired in heart and neural tube, respectively, revealing a role for TIP55 in cellular proliferation. Consistent with these findings, transcriptome profiling revealed perturbations in genes that function in multiple cell types and developmental pathways. These findings show that Tip55 is dispensable for the pre- and early post-implantation roles of Kat5, but is essential during organogenesis. Our results raise the possibility that isoform-specific functions of other chromatin regulatory proteins may play important roles in development.
机译:染色质结构的调节对于细胞类型特异性基因表达至关重要。由于替代性剪接和辅助亚基的不同结合,许多染色质调节复合物以几种不同形式存在。但是,体内研究通常利用消除多种形式复合物的突变,从而无法评估每种复合物的特定作用。在这里,我们检查了KAT5组蛋白乙酰基转移酶的TIP55同工型的发展作用。与缺乏所有四个Kat5转录本的小鼠的植入前致死表型相反,特异缺乏Tip55的小鼠在胚胎第11.5天左右死亡(E11.5)。在发育停滞之前,Tip55突变体胚胎的心脏和神经管有明显缺陷。 Tip55突变体中,心脏和神经细胞命运的说明似乎正常。但是,心脏和神经管中的细胞分裂和存活分别受到损害,从而揭示了TIP55在细胞增殖中的作用。与这些发现一致,转录组谱分析揭示了在多种细胞类型和发育途径中起作用的基因的扰动。这些发现表明,Tip55对于Kat5的植入前和植入后早期作用是必不可少的,但在器官发生过程中是必不可少的。我们的结果提出了其他染色质调节蛋白的同工型特异性功能可能在开发中发挥重要作用的可能性。

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