Wang H Y, Arden K C, Bermingham J R, Viars C S, Lin W, Boyer A D, Fu X D
Department of Medicine, Department of Pathology, University of California at San Diego, 9500 Gilman Drive, La Jolla, California, 92093-0651, USA.
Genomics. 1999 Apr 15;57(2):310-5. doi: 10.1006/geno.1999.5770.
The serine- and arginine-rich (SR) splicing factors play an important role in both constitutive and alternative pre-mRNA splicing, and the functions of these splicing factors are regulated by phosphorylation. We have previously characterized SRPK1 (SFRSK1) and SRPK2 (SFRSK2), which are highly specific protein kinases for the SR family of splicing factors. Here we report the chromosomal localization of the mouse and human genes for both kinases. SRPK1 probes detected two loci that were mapped to mouse Chromosomes 17 and X using The Jackson Laboratory interspecific backcross DNA panel, and SRPK2 probes identified a single locus on mouse Chromosome 5. Using a somatic cell hybrid mapping panel and by fluorescence in situ hybridization, SRPK1 and SRPK2 were respectively mapped to human chromosomes 6p21.2-p21.3 (a region of conserved synteny to mouse Chromosome 17) and 7q22-q31.1 (a region of conserved synteny to mouse Chromosome 5). In addition, we also found multiple SRPK-related sequences on other human chromosomes, one of which appears to correspond to a SRPK2 pseudogene on human chromosome 8.
富含丝氨酸和精氨酸(SR)的剪接因子在组成型和可变前体mRNA剪接中均发挥重要作用,并且这些剪接因子的功能受磷酸化调节。我们之前已对SRPK1(SFRSK1)和SRPK2(SFRSK2)进行了表征,它们是剪接因子SR家族的高度特异性蛋白激酶。在此,我们报告这两种激酶的小鼠和人类基因的染色体定位。使用杰克逊实验室种间回交DNA面板,SRPK1探针检测到两个位点,分别定位于小鼠的17号和X染色体;SRPK2探针在小鼠5号染色体上鉴定出一个单一的位点。利用体细胞杂种定位面板并通过荧光原位杂交,SRPK1和SRPK2分别定位于人类染色体6p21.2 - p21.3(与小鼠17号染色体保守同线性的区域)和7q22 - q31.1(与小鼠5号染色体保守同线性的区域)。此外,我们还在其他人类染色体上发现了多个与SRPK相关的序列,其中一个似乎对应于人类8号染色体上的一个SRPK2假基因。