p57Kip2 expression is enhanced during mid-cardiac murine development and is restricted to trabecular myocardium

Pediatr Res. 1999 May;45(5 Pt 1):635-42. doi: 10.1203/00006450-199905010-00004.


During embryonic development the heart is required to grow in size and cell number, undergo complex morphologic alterations, and function to circulate the blood. Between embryonic d 10.5 (E10.5) and E11.5, cardiac myocytes undergo rapid cell division, resulting in doubling of cardiac mass, while metabolic requirements are increased and contraction force is enhanced. Accelerated cardiomyocyte differentiation is accompanied by a significant increase in trabeculation of ventricular myocardium. Many single gene mutations in the mouse result in a "thinned myocardium" and embryonic lethality between E10.5 and E13.5 secondary to heart failure. This is the case in the Splotch mouse in which a mutation of the Pax3 gene results in neural crest and cardiac defects. Nevertheless, the molecular events governing these important developmental steps remain largely unknown. Here, we describe the use of suppression subtractive hybridization to identify mRNA transcripts whose expression is enhanced during this critical period in normal hearts. These genes encode functions related to maturation of the contractile apparatus, cardiomyocyte differentiation, altered cellular metabolism, and transcriptional regulation. One of the genes that we identified, p57Kip2, encodes a cyclin-dependent kinase inhibitor of the p21 family. We show that p57Kip2 is normally expressed in the inner trabecular layer of the developing heart. In Splotch embryos, expression of p57Kip2 is expanded to encompass the entire thickness of the myocardium. This result and further structural analysis suggests that the myocardial defect of Splotch embryos is associated with precocious cardiomyocyte differentiation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Cell Cycle
  • Cell Differentiation
  • Cell Division
  • Cyclin-Dependent Kinase Inhibitor p57
  • Enzyme Inhibitors
  • Fetal Heart / metabolism
  • Fetal Heart / physiology*
  • Gene Expression Regulation, Developmental*
  • Gestational Age
  • Humans
  • In Situ Hybridization
  • Mice
  • Molecular Sequence Data
  • Myocardium / cytology
  • Myocardium / metabolism*
  • Myocardium / ultrastructure
  • Nuclear Proteins / biosynthesis
  • Nuclear Proteins / chemistry
  • Nuclear Proteins / genetics*
  • Open Reading Frames
  • RNA, Messenger / metabolism
  • Sequence Alignment
  • Sequence Homology, Amino Acid


  • CDKN1C protein, human
  • Cdkn1c protein, mouse
  • Cyclin-Dependent Kinase Inhibitor p57
  • Enzyme Inhibitors
  • Nuclear Proteins
  • RNA, Messenger