Habicher Judith, Haitina Tatjana, Eriksson Inger, Holmborn Katarina, Dierker Tabea, Ahlberg Per E, Ledin Johan
Department of Organismal Biology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
Department of Medical Biochemistry and Microbiology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden.
PLoS One. 2015 Mar 20;10(3):e0121957. doi: 10.1371/journal.pone.0121957. eCollection 2015.
Chondroitin/dermatan sulfate (CS/DS) proteoglycans consist of unbranched sulfated polysaccharide chains of repeating GalNAc-GlcA/IdoA disaccharide units, attached to serine residues on specific proteins. The CS/DS proteoglycans are abundant in the extracellular matrix where they have essential functions in tissue development and homeostasis. In this report a phylogenetic analysis of vertebrate genes coding for the enzymes that modify CS/DS is presented. We identify single orthologous genes in the zebrafish genome for the sulfotransferases chst7, chst11, chst13, chst14, chst15 and ust and the epimerase dse. In contrast, two copies were found for mammalian sulfotransferases CHST3 and CHST12 and the epimerase DSEL, named chst3a and chst3b, chst12a and chst12b, dsela and dselb, respectively. Expression of CS/DS modification enzymes is spatially and temporally regulated with a large variation between different genes. We found that CS/DS 4-O-sulfotransferases and 6-O-sulfotransferases as well as CS/DS epimerases show a strong and partly overlapping expression, whereas the expression is restricted for enzymes with ability to synthesize di-sulfated disaccharides. A structural analysis further showed that CS/DS sulfation increases during embryonic development mainly due to synthesis of 4-O-sulfated GalNAc while the proportion of 6-O-sulfated GalNAc increases in later developmental stages. Di-sulfated GalNAc synthesized by Chst15 and 2-O-sulfated GlcA/IdoA synthesized by Ust are rare, in accordance with the restricted expression of these enzymes. We also compared CS/DS composition with that of heparan sulfate (HS). Notably, CS/DS biosynthesis in early zebrafish development is more dynamic than HS biosynthesis. Furthermore, HS contains disaccharides with more than one sulfate group, which are virtually absent in CS/DS.
硫酸软骨素/硫酸皮肤素(CS/DS)蛋白聚糖由重复的GalNAc-GlcA/IdoA二糖单元组成的无分支硫酸化多糖链构成,这些多糖链连接到特定蛋白质上的丝氨酸残基。CS/DS蛋白聚糖在细胞外基质中含量丰富,在组织发育和内环境稳定中发挥着重要作用。在本报告中,我们对编码修饰CS/DS的酶的脊椎动物基因进行了系统发育分析。我们在斑马鱼基因组中鉴定出硫酸转移酶chst7、chst11、chst13、chst14、chst15和ust以及表异构酶dse的单个直系同源基因。相比之下,哺乳动物硫酸转移酶CHST3和CHST12以及表异构酶DSEL发现有两个拷贝,分别命名为chst3a和chst3b、chst12a和chst12b、dsela和dselb。CS/DS修饰酶的表达在空间和时间上受到调控,不同基因之间存在很大差异。我们发现CS/DS 4-O-硫酸转移酶和6-O-硫酸转移酶以及CS/DS表异构酶表现出强烈且部分重叠的表达,而对于具有合成二硫酸化二糖能力的酶,其表达受到限制。结构分析进一步表明,CS/DS硫酸化在胚胎发育过程中增加,主要是由于4-O-硫酸化GalNAc的合成,而6-O-硫酸化GalNAc的比例在后期发育阶段增加。由Chst15合成的二硫酸化GalNAc和由Ust合成的2-O-硫酸化GlcA/IdoA很少见,这与这些酶的限制性表达一致。我们还将CS/DS的组成与硫酸乙酰肝素(HS)的组成进行了比较。值得注意的是,斑马鱼早期发育中的CS/DS生物合成比HS生物合成更具动态性。此外,HS含有具有多个硫酸基团的二糖,而CS/DS中几乎不存在这些二糖。