Haddad Dania, Puget Nadine, Laviolette-Malirat Nathalie, Conte Caroline, Khamlichi Ahmed Amine
CNRS UMR 5089-IPBS (Institut de Pharmacologie et de Biologie Structurale) and Université Paul Sabatier III; Equipe "Instabilité Génétique et Régulation Transcriptionnelle"; Université de Toulouse; Toulouse, France.
Transcription. 2011 Jul;2(4):183-188. doi: 10.4161/trns.2.4.16784.
In B lymphocytes, class switch recombination (CSR) machinery targets highly repetitive sequences, called switch (S) sequences, in the constant domain of the immunoglobulin heavy chain (IgH) locus. Cotranscriptional generation of R loops at S sequences provides the substrate for the mutagenic enzyme AID (Activation-Induced cytidine Deaminase), which initiates the DNA breaks at the transcribed sequences. Both sense and antisense transcripts across the S regions have been reported. Our recent work shows that, unlike its sense counterpart, antisense transcription of S sequences is dispensable for CSR in vivo.
在B淋巴细胞中,类别转换重组(CSR)机制靶向免疫球蛋白重链(IgH)基因座恒定区中高度重复的序列,即转换(S)序列。S序列处R环的共转录生成提供了诱变酶AID(活化诱导的胞苷脱氨酶)的底物,该酶在转录序列处引发DNA断裂。已有报道称S区域存在正义和反义转录本。我们最近的研究表明,与正义转录本不同,S序列的反义转录在体内对CSR并非必需。