Identification and characterization of the murine ortholog (brms1) of breast-cancer metastasis suppressor 1 (BRMS1).

Academic Article

Abstract

  • We have cloned a novel metastasis-suppressor gene (BRMS1) by differential display, comparing metastatic human breast carcinoma cell line MDA-MB-435 to its metastasis-suppressed human chromosome 11 microcell hybrid. Screening of a murine cDNA library led to the identification of a 1.4 kb cDNA with a sequence revealing 85% homology to human BRMS1 within the open reading frame. The predicted protein sequence for the murine ortholog is 95% identical, suggesting that it is strongly conserved across these 2 species. The cloned cDNA was used to screen a murine strain SV129 BAC library to obtain brms1 genomic DNA. Three BAC clones [226(I4), 226(H4) and 239(N7)] were confirmed to encode the entire brms1 gene. Detailed analysis of BAC clone 226(I4) shows that the gene spans 8.5 kb and, like the human gene, is organized into 10 exons and 9 introns. While the exons share a high degree of homology, there are greater differences when comparing intron structures between the human and murine genes. The 5' upstream region shares about 64% homology with its human counterpart, retaining several of the many putative regulatory elements. Like the human genomic BRMS1, the murine ortholog of the iGnT gene is found upstream of brms1 and the murine ortholog of the RIN1 gene is found downstream of brms1. brms1 was then tested for suppression of metastasis of mouse mammary carcinoma cell line 66cl4 in syngeneic BALB/c mice. Transfection with brms1 did not inhibit 66cl4 primary tumor formation but significantly suppressed its metastatic capability. This suggests that the murine ortholog functions similarly to BRMS1.
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    Published In

    Keywords

  • Amino Acid Sequence, Animals, Blotting, Northern, Chromosomes, Artificial, Bacterial, DNA Primers, Female, Humans, Immunoblotting, Lung Neoplasms, Mammary Neoplasms, Experimental, Mice, Mice, Inbred BALB C, Molecular Sequence Data, Neoplasm Proteins, Proteins, RNA, Messenger, Repressor Proteins, Sequence Homology, Amino Acid, Transfection
  • Digital Object Identifier (doi)

    Pubmed Id

  • 26469947
  • Author List

  • Samant RS; Debies MT; Shevde LA; Verderame MF; Welch DR
  • Start Page

  • 15
  • End Page

  • 20
  • Volume

  • 97
  • Issue

  • 1