Sandulache R, Pretsch W, Chatterjee B, Gimbel W, Graw J, Favor J
Institut für Säugetiergenetik, GSF-Forschungszentrum für Umwelt und Gesundheit, Neuherberg, Oberschleissheim, Germany.
Mamm Genome. 1994 Dec;5(12):777-80. doi: 10.1007/BF00292012.
Four electrophoretic and/or enzyme-activity variants of murine LDH-A subunit (Ldhla-m1Neu, Ldhla-m5Neu, Ldhla-m6Neu, Ldhla-m9Neu), induced by procarbazine hydrochloride or ethylnitrosourea (ENU), were analyzed at the DNA level. The exons of the Ldhl gene from homozygous mutants were amplified by PCR and sequenced. Three mutations resulted from nucleotide substitutions in exon 5: the transitions A-->G at codons 216 (Ldhla-m5Neu) and 225 (Ldhla-m6Neu), and the transversion G-->C (Ldhla-m1Neu) at codon 222. The mutations resulted in the replacements of Glu by Gly (Ldhla-m5Neu), Gln by Arg (Ldhla-m6Neu) and Asp by His (Ldhla-m1Neu). The fourth base substitution, the transition T-->C (Ldhla-m9Neu), has been found at the GT donor splice site following the first exon; this mutation affected the efficiency of transcription. All ENU-induced mutations were A/T-->G/C transitions. The mutation events could be correlated with the biochemical and physiological alterations observed in affected mice.
对由盐酸丙卡巴肼或乙基亚硝基脲(ENU)诱导产生的小鼠乳酸脱氢酶A亚基的四种电泳和/或酶活性变体(Ldhla - m1Neu、Ldhla - m5Neu、Ldhla - m6Neu、Ldhla - m9Neu)进行了DNA水平分析。通过PCR扩增纯合突变体中Ldhl基因的外显子并进行测序。三个突变是由外显子5中的核苷酸替换引起的:密码子216(Ldhla - m5Neu)处的A→G转换、密码子225(Ldhla - m6Neu)处的A→G转换以及密码子222处的G→C颠换(Ldhla - m1Neu)。这些突变导致Glu被Gly取代(Ldhla - m5Neu)、Gln被Arg取代(Ldhla - m6Neu)以及Asp被His取代(Ldhla - m1Neu)。第四个碱基替换,即第一个外显子之后的GT供体剪接位点处的T→C转换(Ldhla - m9Neu),该突变影响了转录效率。所有ENU诱导的突变均为A/T→G/C转换。这些突变事件可能与在受影响小鼠中观察到的生化和生理改变相关。