Human embryonic stem cells express a unique set of microRNAs

Human embryonic stem (hES) cells are pluripotent cell lines established from the explanted inner cell mass of human blastocysts. Despite their importance for human embryology and regenerative medicine, studies on hES cells, unlike those on mouse ES (mES) cells, have been hampered by difficulties in...

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Published inDevelopmental biology Vol. 270; no. 2; pp. 488 - 498
Main Authors Suh, Mi-Ra, Lee, Yoontae, Kim, Jung Yeon, Kim, Soo-Kyoung, Moon, Sung-Hwan, Lee, Ji Yeon, Cha, Kwang-Yul, Chung, Hyung Min, Yoon, Hyun Soo, Moon, Shin Yong, Kim, V.Narry, Kim, Kye-Seong
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 15.06.2004
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Summary:Human embryonic stem (hES) cells are pluripotent cell lines established from the explanted inner cell mass of human blastocysts. Despite their importance for human embryology and regenerative medicine, studies on hES cells, unlike those on mouse ES (mES) cells, have been hampered by difficulties in culture and by scant knowledge concerning the regulatory mechanism. Recent evidence from plants and animals indicates small RNAs of approximately 22 nucleotides (nt), collectively named microRNAs, play important roles in developmental regulation. Here we describe 36 miRNAs (from 32 stem-loops) identified by cDNA cloning in hES cells. Importantly, most of the newly cloned miRNAs are specifically expressed in hES cells and downregulated during development into embryoid bodies (EBs), while miRNAs previously reported from other human cell types are poorly expressed in hES cells. We further show that some of the ES-specific miRNA genes are highly related to each other, organized as clusters, and transcribed as polycistronic primary transcripts. These miRNA gene families have murine homologues that have similar genomic organizations and expression patterns, suggesting that they may operate key regulatory networks conserved in mammalian pluripotent stem cells. The newly identified hES-specific miRNAs may also serve as molecular markers for the early embryonic stage and for undifferentiated hES cells.
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ISSN:0012-1606
1095-564X
DOI:10.1016/j.ydbio.2004.02.019