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编码血小板生成素受体小鼠c-Mpl的基因组位点的结构与转录

Structure and transcription of the genomic locus encoding murine c-Mpl, a receptor for thrombopoietin.

作者信息

Alexander W S, Dunn A R

机构信息

Ludwig Institute for Cancer Research, Royal Melbourne Hospital, Victoria, Australia.

出版信息

Oncogene. 1995 Feb 16;10(4):795-803.

PMID:7862460
Abstract

We have cloned and characterised the murine gene encoding c-Mpl, a receptor for thrombopoietin and member of the hematopoietin receptor superfamily. The gene encompasses 15 kb of the mouse genome and the organisation of its 12 exons conforms closely to the pattern observed for the genes of other hematopoietin receptor family members. A site for initiation of c-mpl transcription was identified 13 nucleotides upstream of the proposed translation initiation codon. The murine mpl promoter sequence lacks conventional TATA and CAAT motifs although the transcription initiation site shares homology with the initiator sequence that specifies transcription initiation in the terminal deoxynucleotidyl transferase gene. The promoter contains consensus binding sequences for several transcriptional regulators including Ets and GATA factors, which have been implicated in control of transcription in megakaryocytes, a cell type that expresses mpl. The generation of multiple transcripts is a feature of the mpl locus. Two distinct mpl transcripts differing by an in-frame insertion of 24 nucleotides were detected in mouse spleen cells. Genomic sequence analysis identified differential splicing of alternative exon 4 sequences as the likely basis for these transcripts, which are predicted to encode receptors which differ within the first Mpl hematopoietin receptor domain.

摘要

我们已经克隆并鉴定了编码c-Mpl的小鼠基因,c-Mpl是血小板生成素的受体,属于造血因子受体超家族成员。该基因包含15kb的小鼠基因组,其12个外显子的组织与其他造血因子受体家族成员基因所观察到的模式紧密相符。在拟翻译起始密码子上游13个核苷酸处鉴定到了c-mpl转录起始位点。小鼠mpl启动子序列缺乏传统的TATA和CAAT基序,尽管转录起始位点与在末端脱氧核苷酸转移酶基因中指定转录起始的起始子序列具有同源性。该启动子包含几个转录调节因子的共有结合序列,包括Ets和GATA因子,它们参与了巨核细胞(一种表达mpl的细胞类型)中的转录控制。产生多种转录本是mpl基因座的一个特征。在小鼠脾细胞中检测到两种不同的mpl转录本,它们相差24个核苷酸的框内插入。基因组序列分析确定外显子4序列的选择性剪接差异是这些转录本的可能基础,预计这些转录本编码在第一个Mpl造血因子受体结构域内不同的受体。

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