Basic Information

Strain name
SD-Erbb3tm1(ERBB3)Bcgen /Bcgen
Common name
B-hHER3 rats
Background
SD rat
Catalog number
113105
Aliases
ErbB-3, FERLK, HER3, LCCS2, MDA-BF-1, VSCN1, c-erbB-3, c-erbB3, erbB3-S, p180-ErbB3, p45-sErbB3, p85-sErbB3
NCBI gene ID
2065

Description

  • HER3, a TAA target, is a member of the epidermal growth factor receptor family and is involved in the regulation of tumor cell growth and differentiation mechanisms. It has been reported that ERBB3 can form heterodimers with other members of the EGFR receptor family, ERBB1 (also known as EGFR, HER1), ERBB2/HER2 and ERBB4/HER4, and activate downstream pathways (PI-3K /Akt, MEK/MAPK, Jak/Stat, etc.). It is involved in the proliferation, differentiation, migration, adhesion, anti-apoptosis and cell transformation of many tumor cells. HER3 is overexpressed in solid tumors such as breast cancer and non-small cell lung cancer, and its downstream signaling pathway is blocked by targeting HER3 antibodies to achieve tumor inhibition, so it becomes an important target for tumor therapy. This target focuses on the development of monoclonal antibodies or drugs coupled with bispecial antibodies or antibodies to members of the same family.
  • Rat Her3 mRNA was only detectable in liver of wild-type rats. Human HER3 mRNA was exclusively detectable in liver of homozygous B-hHER3 rats but not in wild-type rats.

Targeting strategy

Gene targeting strategy for B-hHER3 rats. The exons 1-17 of rats Erbb3 gene that encode extracellular domain and transmembrane domain is replaced by human counterparts in B-hHER3 rats. The genomic region of rat Erbb3 gene that encodes signal peptide and cytoplasmic portion is retained. The promoter, 5’UTR and 3’UTR region of the rat gene are also retained. The chimeric HER3 expression is driven by endogenous rat Erbb3 promoter, while rat Erbb3 gene transcription and translation will be disrupted.

mRNA expression analysis

Strain specific analysis of HER3 mRNA expression in wild-type SD rats and B-hHER3 rats by RT-PCR. Liver RNA were isolated from wild-type SD rats (+/+) and homozygous B-hHER3 rats (H/H), then cDNA libraries were synthesized by reverse transcription, followed by PCR with rat or human HER3 primers. Rat Her3 mRNA was only detectable in wild-type rats. Human HER3 mRNA was exclusively detectable in homozygous B-hHER3 rats but not in wild-type rats.

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