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. Author manuscript; available in PMC: 2019 Aug 16.
Published in final edited form as: J Cell Biochem. 2012 Apr;113(4):1265–1273. doi: 10.1002/jcb.23459

Fig. 3.

Fig. 3.

Splicing analysis of titin mRNA in wild type and mutant skeletal muscles. cDNAs from Wt TA, Hm TA, Wt LD, and Hm LD are amplified by primer sets: 50F-59R, 59F-71R, 71F-84R, 84F-96R 96F-115R, 115F-137R, 137F-156R, and 156F-226R for the corresponding exons (Ex, exon; F, forward primer; R, reverse primer). A: only constitutive splicing can be found in the middle Ig region (exon 50-115) of Hm TA, Wt LD, and Hm LD. B: alternative splicing of middle Ig region can be found in Wt TA but only constitutive splicing in Hm TA. C: Only alternative splicing can be detected in the PEVK region (exon 115-226) of Wt TA but constitutive splicing exists in wt LD, Hm LD, and Hm TA from exon 115 to 156; the region from exon 156 to 226 is alternatively spliced in all tested tissues.