Multiple alternative splicing forms of human RAD17 and their differential response to ionizing radiation

Citation
Ms. Chen et al., Multiple alternative splicing forms of human RAD17 and their differential response to ionizing radiation, GENE, 277(1-2), 2001, pp. 145-152
Citations number
15
Categorie Soggetti
Molecular Biology & Genetics
Journal title
GENE
ISSN journal
03781119 → ACNP
Volume
277
Issue
1-2
Year of publication
2001
Pages
145 - 152
Database
ISI
SICI code
0378-1119(20011017)277:1-2<145:MASFOH>2.0.ZU;2-V
Abstract
In this study, we have identified four alternatively spliced RAD17 RNAs, FM 1, FM2, FM3, and FM4, which are produced through alternative splicing withi n the first 300 base-pairs of the coding region. FM3 and FM4 are two novel forms that have not been reported before. All four alternatively spliced RA D17 RNAs were detected in the tissues we exantined. However, the levels of these forms varied from tissue to tissue. The expression of these four form s was also found to differ in different phases of the cell cycle and follow ing exposure to X-irradiation. FM2, FM1, FM4, and FM3 encode putative polyp eptides consisting of 681, 670, 596, and 516 amino acids, respectively, To determine if these polypeptides were expressed in cells, we generated a pol yclonal antibody using a synthetic peptide. A major band around 71 kDa and two minor bands around 73 and 62 kDa were detected in human normal fibrobla sts on Western blots. These three bands appear to represent the proteins en coded by FM2 (the 73 kDa band), FM1 (the 71 kDa band), and FM4 (the 62 kDa band) since the apparent molecular weights are close to their theoretical w eights of the predicted amino acid sequences. The abundance of the 71 kDa. protein was not significantly affected by X-irradiation, while the abundanc e of the 73 and the 62 kDa proteins was increased at least 5-fold 14 h post irradiation. The differential expression of these four alternatively splice d forms in different tissues, in different phases of the cell cycle, and th eir differential response to X-irradiation suggest that they may perform di fferent functions in cell-cycle regulation and in the response to irradiati on. (C) 2001 Elsevier Science B.V. All rights reserved.