Grb7 knockout mice develop normally but litters born to knockout females fail to thrive.

Background: Growth factor receptor‐bound 7 (Grb7) is an adaptor protein involved in signal transduction downstream of multiple receptor tyrosine kinases, including ERBB, FGFR, and PDGFR pathways. Experimental studies have implicated Grb7 in regulating cell proliferation, survival, migration, and invasion through its large repertoire of protein–protein interactions. Results: Here, we describe the generation and characterization of a Grb7 knockout mouse. These mice are viable and fertile. A lacZ knock‐in reporter was used to visualize Grb7 promoter activity patterns in adult tissues, indicating widespread Grb7 expression in glandular epithelium, the central nervous system, and other tissues. The sole defect observed in these animals was a failure of Grb7 knockout females to successfully raise pups to weaning age, a phenotype that was independent of both paternal and pup genotypes. Conclusions: These data suggest a regulatory role for Grb7 in mammary lactational physiology. Key Findings: Despite many reports implicating Grb7 in multiple signal transduction pathways, deletion of this signaling adapter protein had minimal effects on mouse development.Grb7 knockout animals were viable and fertile but knockout females were deficient in the ability to raise pups to weaning age.These data imply a requirement for Grb7 in lactational sufficiency. [ABSTRACT FROM AUTHOR]