Abstract
Background. Rex1/Zfp42 has been extensively used as a marker for the undifferentiated state of pluripotent stem cells. However, its function in pluripotent stem cells including embryonic stem (ES) cells remained unclear although its involvement in visceral endoderm differentiation in F9 embryonal carcinoma (EC) cells was reported. Results. We showed the function of Rex1 in mouse ES cells as well as in embryos using the conventional gene targeting strategy. Our results clearly indicated that Rex1 function is dispensable for both the maintenance of pluripotency in ES cells and the development of embryos. However, Rex1-/- ES cells showed the defect to induce a subset of the marker genes of visceral endoderm, when differentiated as embryoid body, as found in EC cells. Conclusion. Rex1 should be regarded just as a marker of pluripotency without functional significance like the activity of alkaline phosphatase.
| Original language | English |
|---|---|
| Article number | 45 |
| Journal | BMC Developmental Biology |
| Volume | 8 |
| DOIs | |
| Publication status | Published - 2008 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Medicine(all)
Cite this
Rex1/Zfp42 is dispensable for pluripotency in mouse ES cells. / Masui, Shinji; Ohtsuka, Satoshi; Yagi, Rika; Takahashi, Kadue; Ko, Minoru; Niwa, Hitoshi.
In: BMC Developmental Biology, Vol. 8, 45, 2008.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Rex1/Zfp42 is dispensable for pluripotency in mouse ES cells
AU - Masui, Shinji
AU - Ohtsuka, Satoshi
AU - Yagi, Rika
AU - Takahashi, Kadue
AU - Ko, Minoru
AU - Niwa, Hitoshi
PY - 2008
Y1 - 2008
N2 - Background. Rex1/Zfp42 has been extensively used as a marker for the undifferentiated state of pluripotent stem cells. However, its function in pluripotent stem cells including embryonic stem (ES) cells remained unclear although its involvement in visceral endoderm differentiation in F9 embryonal carcinoma (EC) cells was reported. Results. We showed the function of Rex1 in mouse ES cells as well as in embryos using the conventional gene targeting strategy. Our results clearly indicated that Rex1 function is dispensable for both the maintenance of pluripotency in ES cells and the development of embryos. However, Rex1-/- ES cells showed the defect to induce a subset of the marker genes of visceral endoderm, when differentiated as embryoid body, as found in EC cells. Conclusion. Rex1 should be regarded just as a marker of pluripotency without functional significance like the activity of alkaline phosphatase.
AB - Background. Rex1/Zfp42 has been extensively used as a marker for the undifferentiated state of pluripotent stem cells. However, its function in pluripotent stem cells including embryonic stem (ES) cells remained unclear although its involvement in visceral endoderm differentiation in F9 embryonal carcinoma (EC) cells was reported. Results. We showed the function of Rex1 in mouse ES cells as well as in embryos using the conventional gene targeting strategy. Our results clearly indicated that Rex1 function is dispensable for both the maintenance of pluripotency in ES cells and the development of embryos. However, Rex1-/- ES cells showed the defect to induce a subset of the marker genes of visceral endoderm, when differentiated as embryoid body, as found in EC cells. Conclusion. Rex1 should be regarded just as a marker of pluripotency without functional significance like the activity of alkaline phosphatase.
UR - http://www.scopus.com/inward/record.url?scp=44049089423&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=44049089423&partnerID=8YFLogxK
U2 - 10.1186/1471-213X-8-45
DO - 10.1186/1471-213X-8-45
M3 - Article
C2 - 18433507
AN - SCOPUS:44049089423
VL - 8
JO - BMC Developmental Biology
JF - BMC Developmental Biology
SN - 1471-213X
M1 - 45
ER -