Organization, structure and alternate splicing of the murine RFC-1 gene encoding a folate transporter.
Organization, structure and alternate splicing of the murine RFC-1 gene encoding a folate transporter.
复制标题
编码叶酸转运蛋白的鼠 RFC-1 基因的组织、结构和可变剪接。
DOI:
10.1016/s0378-1119(96)00676-2
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发表时间:
1997
期刊:
影响因子:
3.5
通讯作者:
Sirotnak,FM
中科院分区:
文献类型:
--
作者:
Tolner,B;Roy,K;Sirotnak,FM
The structural organization of the murine RFC-1 gene encoding a folate transporter has been determined. The entire nucleotide sequence of the L1210 cell RFC-1 cDNA, the 3′- and 5′-untranslated regions and the coding sequence were found to be distributed in eight exons, including six primary exons and alternates to exon 1 and exon 5, spanning 10.4 kb. Splice variants were identified in an L1210 cell cDNA library. The most common incorporates exons 1 through 6, encoding a 58-kDa polypeptide. The two least common incorporate exons 1 and 2, a truncated version of exon 3 and exons 4 through 6; or exons 1 through 4, an alternate to exon 5, and exon 6, encoding polypeptides of 53.6 and 43.4 kDa, respectively. A fourth variant reported earlier (GenBank/EMBL accession No. L36539) by others incorporates what we have found to be an alternate of exon 1 and exons 2 through 6. A relatively GC-rich region of the genome just 5′ of exon 1 as well as exon 1a appears to be distinctly promoter-like and encodes a number of putative cis-acting elements. The findings pertaining to alternates of exon 1 suggest that the transcription of RFC-1 variants results from two different promoters. © 1997 Elsevier Science B.V. All rights reserved.