Snider Paige L, Snider Elizabeth, Simmons Olga, Lilly Brenda, Conway Simon J
HB Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Biosciences, Indiana University, Bloomington, IN 47405, USA.
J Cardiovasc Dev Dis. 2019 Jun 22;6(2):24. doi: 10.3390/jcdd6020024.
Mammalian and are a homologous pair of uncharacterized, highly conserved genes cloned from fetal and adult brain cDNA libraries. Herein we map the spatiotemporal expression of and mRNA and their expression patterns in postnatal testis, skin, gastrointestinal, and adipose progenitor tissues. Significantly, is present throughout the early stages of mouse heart development, particularly in the second heart field (SHF) lineage as it differentiates from mesenchymal cells into cardiomyocytes. We also show that is expressed within several early neuronal tissues destined to give rise to central, peripheral, and sympathetic nervous system structures. Expression profiling revealed that the paralog is not expressed during the normal developmental process and that expression was noticeably absent from most adult terminally differentiated tissues. Finally, we confirm that a previously uncharacterized CRISPR/CAS-generated mouse mutant allele is hypomorphic.
哺乳动物的[基因名称1]和[基因名称2]是一对同源的未表征的、高度保守的基因,它们是从胎儿和成人脑cDNA文库中克隆出来的。在此,我们绘制了[基因名称1]和[基因名称2] mRNA在时空上的表达情况以及它们在出生后睾丸、皮肤、胃肠道和脂肪祖细胞组织中的表达模式。值得注意的是,[基因名称1]在小鼠心脏发育的早期阶段均有表达,特别是在第二心脏场(SHF)谱系中,因为它从间充质细胞分化为心肌细胞。我们还表明,[基因名称1]在一些早期神经元组织中表达,这些组织注定会产生中枢、外周和交感神经系统结构。表达谱分析显示,旁系同源基因[基因名称2]在正常发育过程中不表达,并且在大多数成年终末分化组织中明显不存在[基因名称1]的表达。最后,我们证实了一个先前未表征的由CRISPR/CAS产生的[基因名称1]小鼠突变等位基因是亚效等位基因。