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在哺乳动物心脏发育过程中,Casz1是心肌细胞从G1期进入S期所必需的。

Casz1 is required for cardiomyocyte G1-to-S phase progression during mammalian cardiac development.

作者信息

Dorr Kerry M, Amin Nirav M, Kuchenbrod Lauren M, Labiner Hanna, Charpentier Marta S, Pevny Larysa H, Wessels Andy, Conlon Frank L

机构信息

University of North Carolina McAllister Heart Institute, UNC-Chapel Hill, Chapel Hill, NC 27599-3280, USA Department of Genetics, UNC-Chapel Hill, Chapel Hill, NC 27599-3280, USA.

Department of Biology, UNC-Chapel Hill, Chapel Hill, NC 27599-3280, USA.

出版信息

Development. 2015 Jun 1;142(11):2037-47. doi: 10.1242/dev.119107. Epub 2015 May 7.

Abstract

Organ growth occurs through the integration of external growth signals during the G1 phase of the cell cycle to initiate DNA replication. Although numerous growth factor signals have been shown to be required for the proliferation of cardiomyocytes, genetic studies have only identified a very limited number of transcription factors that act to regulate the entry of cardiomyocytes into S phase. Here, we report that the cardiac para-zinc-finger protein CASZ1 is expressed in murine cardiomyocytes. Genetic fate mapping with an inducible Casz1 allele demonstrates that CASZ1-expressing cells give rise to cardiomyocytes in the first and second heart fields. We show through the generation of a cardiac conditional null mutation that Casz1 is essential for the proliferation of cardiomyocytes in both heart fields and that loss of Casz1 leads to a decrease in cardiomyocyte cell number. We further report that the loss of Casz1 leads to a prolonged or arrested S phase, a decrease in DNA synthesis, an increase in phospho-RB and a concomitant decrease in the cardiac mitotic index. Taken together, these studies establish a role for CASZ1 in mammalian cardiomyocyte cell cycle progression in both the first and second heart fields.

摘要

器官生长通过细胞周期G1期外部生长信号的整合来启动DNA复制。尽管已表明许多生长因子信号是心肌细胞增殖所必需的,但遗传学研究仅鉴定出非常有限数量的转录因子,它们可调节心肌细胞进入S期。在此,我们报告心脏类锌指蛋白CASZ1在小鼠心肌细胞中表达。利用可诱导的Casz1等位基因进行的遗传命运图谱分析表明,表达CASZ1的细胞在第一和第二心脏区域产生心肌细胞。我们通过产生心脏条件性无效突变表明,Casz1对于两个心脏区域中心肌细胞的增殖至关重要,并且Casz1的缺失导致心肌细胞数量减少。我们进一步报告,Casz1的缺失导致S期延长或停滞、DNA合成减少、磷酸化RB增加以及心脏有丝分裂指数随之降低。综上所述,这些研究确立了CASZ1在第一和第二心脏区域哺乳动物心肌细胞周期进程中的作用。

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