Wang Liangli, Wansleeben Carolien, Zhao Shengli, Miao Pei, Paschen Wulf, Yang Wei
Multidisciplinary Neuroprotection Laboratories, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Department of Cell Biology, Duke University Medical Center, Durham, NC, USA.
EMBO Rep. 2014 Aug;15(8):878-85. doi: 10.15252/embr.201438534. Epub 2014 Jun 2.
Small ubiquitin-like modifier (SUMO1-3) conjugation plays a critical role in embryogenesis. Embryos deficient in the SUMO-conjugating enzyme Ubc9 die at the early postimplantation stage. Sumo1(-/-) mice are viable, as SUMO2/3 can compensate for most SUMO1 functions. To uncover the role of SUMO2/3 in embryogenesis, we generated Sumo2- and Sumo3-null mutant mice. Here, we report that Sumo3(-/-) mice were viable, while Sumo2(-/-) embryos exhibited severe developmental delay and died at approximately embryonic day 10.5 (E10.5). We also provide evidence that SUMO2 is the predominantly expressed SUMO isoform. Furthermore, although Sumo2(+/-) and Sumo2(+/-);Sumo3(+/-) mice lacked any overt phenotype, only 2 Sumo2(+/-);Sumo3(-/-) mice were found at birth in 35 litters after crossing Sumo2(+/-);Sumo3(+/-) with Sumo3(-/-) mice, and these rare mice were considerably smaller than littermates of the other genotypes. Thus, our findings suggest that expression levels and not functional differences between SUMO2 and SUMO3 are critical for normal embryogenesis.
小泛素样修饰物(SUMO1 - 3)缀合在胚胎发生中起关键作用。缺乏SUMO缀合酶Ubc9的胚胎在植入后早期死亡。Sumo1(-/-)小鼠是可存活的,因为SUMO2/3可以补偿大多数SUMO1的功能。为了揭示SUMO2/3在胚胎发生中的作用,我们构建了Sumo2和Sumo3基因敲除突变小鼠。在此,我们报告Sumo3(-/-)小鼠可存活,而Sumo2(-/-)胚胎表现出严重的发育延迟,并在大约胚胎第10.5天(E10.5)死亡。我们还提供证据表明SUMO2是主要表达的SUMO异构体。此外,尽管Sumo2(+/-)和Sumo2(+/-);Sumo3(+/-)小鼠没有任何明显的表型,但将Sumo2(+/-);Sumo3(+/-)与Sumo3(-/-)小鼠杂交后,在35窝出生的小鼠中仅发现2只Sumo2(+/-);Sumo3(-/-)小鼠,这些罕见的小鼠比其他基因型的同窝小鼠小得多。因此,我们的研究结果表明,SUMO2和SUMO3之间的表达水平而非功能差异对正常胚胎发生至关重要。