Essalmani Rachid, Zaid Ahmed, Marcinkiewicz Jadwiga, Chamberland Ann, Pasquato Antonella, Seidah Nabil G, Prat Annik
Laboratory of Biochemical Neuroendocrinology, Clinical Research Institute of Montreal, 110 Pine Avenue West, Montreal, QC, Canada.
Proc Natl Acad Sci U S A. 2008 Apr 15;105(15):5750-5. doi: 10.1073/pnas.0709428105. Epub 2008 Mar 31.
The proprotein convertase PC5/6 cleaves protein precursors after basic amino acids and is essential for implantation in CD1/129/Sv/C57BL/6 mixed-background mice. Conditional inactivation of Pcsk5 in the epiblast but not in the extraembryonic tissue bypassed early embryonic lethality but resulted in death at birth. PC5/6-deficient embryos exhibited Gdf11-related phenotypes such as altered anteroposterior patterning with extra vertebrae and lack of tail and kidney agenesis. They also exhibited Gdf11-independent phenotypes, such as a smaller size, multiple hemorrhages, collapsed alveoli, and retarded ossification. In situ hybridization revealed overlapping PC5/6 and Gdf11 mRNA expression patterns. In vitro and ex vivo analyses showed that the selectivity of PC5/6 for Gdf11 essentially resides in the presence of a P1' Asn in the RSRR downward arrowN cleavage motif. This work identifies Gdf11 as a likely in vivo specific substrate of PC5/6 and opens the way to the identification of other key substrates of this convertase.
前蛋白转化酶PC5/6在碱性氨基酸之后切割蛋白质前体,对于CD1/129/Sv/C57BL/6混合背景小鼠的着床至关重要。在胚泡中而非胚外组织中条件性失活Pcsk5可绕过早期胚胎致死性,但导致出生时死亡。PC5/6缺陷型胚胎表现出与Gdf11相关的表型,如前后模式改变、椎骨增多、无尾和肾缺如。它们还表现出与Gdf11无关的表型,如体型较小、多处出血、肺泡塌陷和骨化延迟。原位杂交显示PC5/6和Gdf11 mRNA表达模式重叠。体外和离体分析表明,PC5/6对Gdf11的选择性主要在于RSRR↓N切割基序中P1'位天冬酰胺的存在。这项工作确定Gdf11可能是PC5/6在体内的特异性底物,并为鉴定该转化酶的其他关键底物开辟了道路。