Acute Myeloid Leukemia-Associated Mkl1 (Mrtf-a) Is a Key Regulator of Mammary Gland Function

Author:

Sun Yi1,Boyd Kelli2,Xu Wu3,Ma Jing4,Jackson Carl W.5,Fu Amina1,Shillingford Jonathan M.6,Robinson Gertraud W.6,Hennighausen Lothar6,Hitzler Johann K.7,Ma Zhigui1,Morris Stephan W.15

Affiliation:

1. Department of Pathology

2. Animal Resource Center

3. Department of Biochemistry

4. Hartwell Center for Bioinformatics and Biotechnology

5. Department of Hematology-Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105

6. Laboratory of Genetics and Physiology, National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, Maryland 20892

7. Department of Paediatrics, Division of Haematology/Oncology, Program in Developmental Biology, The Hospital for Sick Children, Toronto, Ontario M5G 1X8, Canada

Abstract

ABSTRACT Transcription of immediate-early genes—as well as multiple genes affecting muscle function, cytoskeletal integrity, apoptosis control, and wound healing/angiogenesis—is regulated by serum response factor (Srf). Extracellular signals regulate Srf in part via a pathway involving megakaryoblastic leukemia 1 (Mkl1, also known as myocardin-related transcription factor A [Mrtf-a]), which coactivates Srf-responsive genes downstream of Rho GTPases. Here we investigate Mkl1 function using gene targeting and show the protein to be essential for the physiologic preparation of the mammary gland during pregnancy and the maintenance of lactation. Lack of Mkl1 causes premature involution and impairs expression of Srf-dependent genes in the mammary myoepithelial cells, which control milk ejection following oxytocin-induced contraction. Despite the importance of Srf in multiple transcriptional pathways and widespread Mkl1 expression, the spectrum of abnormalities associated with Mkl1 absence appears surprisingly restricted.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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