Sucov H M, Hough-Evans B R, Franks R R, Britten R J, Davidson E H
Division of Biology, California Institute of Technology, Pasadena 91125.
Genes Dev. 1988 Oct;2(10):1238-50. doi: 10.1101/gad.2.10.1238.
DNA sequences derived from the 5' region of a gene coding for the 50-kD skeletal matrix protein (SM50) of sea urchin embryo spicules were linked to the CAT reporter gene and injected into unfertilized eggs. CAT mRNA and enzyme were synthesized from these fusion constructs in embryos derived from these eggs, and in situ hybridization with a CAT antisense RNA probe demonstrated that expression is confined to skeletogenic mesenchyme cells. A mean of 5.5 of the 32-blastula-stage skeletogenic mesenchyme cells displayed CAT mRNA (range 1-15), a result consistent with earlier measurements indicating that incorporation of the exogenous injected DNA probably occurs in a single blastomere during early cleavage. In vitro mutagenesis and deletion experiments showed that CAT enzyme activity in the transgenic embryos is enhanced 34-fold by decreasing the number of SM50 amino acids at the amino-terminus of the fusion protein from 43 to 4. cis-regulatory sequences that are sufficient to promote lineage-specific spatial expression in the embryo are located between -440 and +120 with respect to the transcriptional initiation site.
从编码海胆胚胎针状体50-kD骨骼基质蛋白(SM50)的基因5'区域获得的DNA序列与CAT报告基因相连,并注射到未受精卵中。在这些卵发育而来的胚胎中,这些融合构建体合成了CAT mRNA和酶,并且用CAT反义RNA探针进行原位杂交表明,表达仅限于造骨间充质细胞。在32细胞囊胚期的造骨间充质细胞中,平均有5.5个细胞显示出CAT mRNA(范围为1 - 15),这一结果与早期测量结果一致,表明外源注射的DNA可能在早期卵裂期间于单个卵裂球中整合。体外诱变和缺失实验表明,通过将融合蛋白氨基末端的SM50氨基酸数量从43个减少到4个,转基因胚胎中的CAT酶活性提高了34倍。相对于转录起始位点,足以促进胚胎中谱系特异性空间表达的顺式调控序列位于 - 440至 + 120之间。