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作 者:Alan Chant Ahmad Chaudary Christina M. Kraemer-Chant Alan Chant;Ahmad Chaudary;Christina M. Kraemer-Chant(Department of Chemistry, Saint Michael’s College, Colchester, VT, USA;Bowling Green State University, Bowling Green, OH, USA)
机构地区:[1]Department of Chemistry, Saint Michael’s College, Colchester, VT, USA [2]Bowling Green State University, Bowling Green, OH, USA
出 处:《Advances in Biological Chemistry》2023年第4期128-142,共15页生物化学进展(英文)
摘 要:Multiplex Ligation-Dependent Probe Amplification (MLPA) was used to study the integrity of the chromosomes for two WIL2-derived lymphoblastoid cell lines (TK6 and WTK1) in the presence and absence of ionizing radiation. WTK1 cells contain a p53 mutation, whereas the TK6 cell line has the native p53 tumor-suppressor gene. Each cell line was isolated pre- and post-irradiation (2 and 3 Gy) and analyzed by MLPA. Using probes that target specific regions on chromosomes associated with a distinct subset of microdeletions and microduplications either established or thought to be responsible for intellectual disability or developmental delay, we have demonstrated that WTK1 and TK6 are not impacted in the same way by irradiation. Instead, each cell line presents its own unique MLPA profile. The most notable differences are the appearance of nine unique probe signals only seen in WTK1 cells. These results are important in the study of how different cell lines can be affected in significantly different ways depending on the presence or absence of wild type p53.Multiplex Ligation-Dependent Probe Amplification (MLPA) was used to study the integrity of the chromosomes for two WIL2-derived lymphoblastoid cell lines (TK6 and WTK1) in the presence and absence of ionizing radiation. WTK1 cells contain a p53 mutation, whereas the TK6 cell line has the native p53 tumor-suppressor gene. Each cell line was isolated pre- and post-irradiation (2 and 3 Gy) and analyzed by MLPA. Using probes that target specific regions on chromosomes associated with a distinct subset of microdeletions and microduplications either established or thought to be responsible for intellectual disability or developmental delay, we have demonstrated that WTK1 and TK6 are not impacted in the same way by irradiation. Instead, each cell line presents its own unique MLPA profile. The most notable differences are the appearance of nine unique probe signals only seen in WTK1 cells. These results are important in the study of how different cell lines can be affected in significantly different ways depending on the presence or absence of wild type p53.
关 键 词:Ionizing Radiation Multiplex Ligation-Dependent Probe Amplification (MLPA) Intellectual Disability (ID) Developmental Delay (DD) p53 Tumor Suppressor
分 类 号:R11[医药卫生—公共卫生与预防医学]
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