TY - JOUR
T1 - Alternative SET/TAFI Promoters Regulate Embryonic Stem Cell Differentiation
AU - Edupuganti, Raghu Ram
AU - Harikumar, Arigela
AU - Aaronson, Yair
AU - Biran, Alva
AU - Sailaja, Badi Sri
AU - Nissim-Rafinia, Malka
AU - Azad, Gajendra Kumar
AU - Cohen, Malkiel A.
AU - Park, Jung Eun
AU - Shivalila, Chikdu S.
AU - Markoulaki, Styliani
AU - Sze, Siu Kwan
AU - Jaenisch, Rudolf
AU - Meshorer, Eran
N1 - Publisher Copyright:
© 2017 The Authors
PY - 2017/10/10
Y1 - 2017/10/10
N2 - Embryonic stem cells (ESCs) are regulated by pluripotency-related transcription factors in concert with chromatin regulators. To identify additional stem cell regulators, we screened a library of endogenously labeled fluorescent fusion proteins in mouse ESCs for fluorescence loss during differentiation. We identified SET, which displayed a rapid isoform shift during early differentiation from the predominant isoform in ESCs, SETα, to the primary isoform in differentiated cells, SETβ, through alternative promoters. SETα is selectively bound and regulated by pluripotency factors. SET depletion causes proliferation slowdown and perturbed neuronal differentiation in vitro and developmental arrest in vivo, and photobleaching methods demonstrate SET's role in maintaining a dynamic chromatin state in ESCs. This work identifies an important regulator of pluripotency and early differentiation, which is controlled by alternative promoter usage. In this article, Meshorer and colleagues screen the endogenously tagged fluorescent library they generated (see the accompanying paper by Harikumar et al.) and identify a linker histone chaperone, SET/TAF-I, to be involved in regulating mouse ESC pluripotency and early differentiation decisions. They show that SET has two isoforms regulated by alternative promoters and pluripotency factors, which are switched during early differentiation. SETα/SETβ replacement is important for ESC differentiation.
AB - Embryonic stem cells (ESCs) are regulated by pluripotency-related transcription factors in concert with chromatin regulators. To identify additional stem cell regulators, we screened a library of endogenously labeled fluorescent fusion proteins in mouse ESCs for fluorescence loss during differentiation. We identified SET, which displayed a rapid isoform shift during early differentiation from the predominant isoform in ESCs, SETα, to the primary isoform in differentiated cells, SETβ, through alternative promoters. SETα is selectively bound and regulated by pluripotency factors. SET depletion causes proliferation slowdown and perturbed neuronal differentiation in vitro and developmental arrest in vivo, and photobleaching methods demonstrate SET's role in maintaining a dynamic chromatin state in ESCs. This work identifies an important regulator of pluripotency and early differentiation, which is controlled by alternative promoter usage. In this article, Meshorer and colleagues screen the endogenously tagged fluorescent library they generated (see the accompanying paper by Harikumar et al.) and identify a linker histone chaperone, SET/TAF-I, to be involved in regulating mouse ESC pluripotency and early differentiation decisions. They show that SET has two isoforms regulated by alternative promoters and pluripotency factors, which are switched during early differentiation. SETα/SETβ replacement is important for ESC differentiation.
KW - SET
KW - TAF-I
KW - TAFI
KW - chromatin
KW - differentiation
KW - embryonic stem cells
KW - epigenetics
KW - histone chaperone
KW - histone dynamics
KW - pluripotency
UR - http://www.scopus.com/inward/record.url?scp=85030696288&partnerID=8YFLogxK
U2 - 10.1016/j.stemcr.2017.08.021
DO - 10.1016/j.stemcr.2017.08.021
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C2 - 28966118
AN - SCOPUS:85030696288
SN - 2213-6711
VL - 9
SP - 1291
EP - 1303
JO - Stem Cell Reports
JF - Stem Cell Reports
IS - 4
ER -