TY - JOUR
T1 - Cytoplasmic poly (A)-binding protein critically regulates epidermal maintenance and turnover in the planarian schmidtea mediterranea
AU - Bansal, Dhiru
AU - Kulkarni, Jahnavi
AU - Nadahalli, Kavana
AU - Lakshmanan, Vairavan
AU - Krishna, Srikar
AU - Sasidharan, Vidyanand
AU - Geo, Jini
AU - Dilipkumar, Shilpa
AU - Pasricha, Renu
AU - Gulyani, Akash
AU - Raghavan, Srikala
AU - Palakodeti, Dasaradhi
N1 - Publisher Copyright:
© 2017. Published by The Company of Biologists Ltd.
PY - 2017/9/1
Y1 - 2017/9/1
N2 - Identifying key cellular events that facilitate stem cell function and tissue organization is crucial for understanding the process of regeneration. Planarians are powerful model system to study regeneration and stem cell (neoblast) function. Here, using planaria, we show that the initial events of regeneration, such as epithelialization and epidermal organization are critically regulated by a novel cytoplasmic poly A-binding protein, SMED-PABPC2. Knockdown of smed-pabpc2 leads to defects in epidermal lineage specification, disorganization of epidermis and ECM, and deregulated wound healing, resulting in the selective failure of neoblast proliferation near the wound region. Polysome profiling suggests that epidermal lineage transcripts, including zfp-1, are translationally regulated by SMED-PABPC2. Together, our results uncover a novel role for SMED-PABPC2 in the maintenance of epidermal and ECM integrity, critical for wound healing and subsequent processes for regeneration.
AB - Identifying key cellular events that facilitate stem cell function and tissue organization is crucial for understanding the process of regeneration. Planarians are powerful model system to study regeneration and stem cell (neoblast) function. Here, using planaria, we show that the initial events of regeneration, such as epithelialization and epidermal organization are critically regulated by a novel cytoplasmic poly A-binding protein, SMED-PABPC2. Knockdown of smed-pabpc2 leads to defects in epidermal lineage specification, disorganization of epidermis and ECM, and deregulated wound healing, resulting in the selective failure of neoblast proliferation near the wound region. Polysome profiling suggests that epidermal lineage transcripts, including zfp-1, are translationally regulated by SMED-PABPC2. Together, our results uncover a novel role for SMED-PABPC2 in the maintenance of epidermal and ECM integrity, critical for wound healing and subsequent processes for regeneration.
KW - Epidermis
KW - Neoblast
KW - Planaria
KW - Poly (A)-binding proteins
KW - Regeneration
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U2 - 10.1242/dev.152942
DO - 10.1242/dev.152942
M3 - Article
C2 - 28807897
AN - SCOPUS:85028605335
SN - 0950-1991
VL - 144
SP - 3066
EP - 3079
JO - Development (Cambridge)
JF - Development (Cambridge)
IS - 17
ER -