https://transhumanist.ru/index.php?action=history&feed=atom&title=FANCD2 2026-06-23T01:09:11Z История изменений этой страницы в вики MediaWiki 1.43.6 https://transhumanist.ru/index.php?title=FANCD2&diff=6529&oldid=prev 2021-05-12T15:35:26Z

<p>Новая страница: «Fanconi anemia group D2 protein (Protein FACD2) [FACD] ==Publications== {{medline-entry |title=<a href="/TFG" title="TFG">TFG</a>-maintaining stability of overlooked <a href="/FANCD2" title="FANCD2">FANCD2</a> confers ea...»</p> <p><b>Новая страница</b></p><div>Fanconi anemia group D2 protein (Protein FACD2) [FACD]<br /> <br /> ==Publications==<br /> <br /> {{medline-entry<br /> |title=[[TFG]]-maintaining stability of overlooked [[FANCD2]] confers early DNA-damage response.<br /> |pubmed-url=https://pubmed.ncbi.nlm.nih.gov/33099537<br /> |abstract=Emerging Fanconi Anemia (FA) signaling in the field of cancer research annotates the extreme importance of its center player, Fanconi Anemia complementation group D2 ([[FANCD2]]) in protecting human cells from going awry. However, a previously-unrecognized form of [[FANCD2]], namely [[FANCD2]]-V2, is understudied. We report TRK-Fused Gene ([[TFG]]) is critical for roles played by [[FANCD2]]-V2 in early responses to DNA damage, but not for [[FANCD2]]-V1, the long-known form of [[FANCD2]]. [[FANCD2]]-V2 forms nuclear foci upon DNA damage, and both its focus appearance and disappearance are earlier than [[FANCD2]]-V1. The amino acid/aa 5-100 of [[TFG]] and the aa1437-1442 of [[FANCD2]]-V2 were identified to contribute to their interaction, which maintains the steady-state level of [[FANCD2]]-V2 protein. [[TFG]]Δaa5-100 or [[FANCD2]]-V2Δaa1437-1442-carrying cells could not show timely focus formation of [[FANCD2]]-V2 upon DNA damage and gained carcinogenicity over time. This study provides a previously-unknown key to unlock in-depth insights into maintaining genome stability, fostering translational studies on preventing, diagnosing and/or treating related diseases.<br /> <br /> |keywords=* DNA damage response<br /> * FANCD2<br /> * TFG<br /> * aging and cancer<br /> |full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655164<br /> }}<br /> {{medline-entry<br /> |title=[[FANCD2]] and DNA Damage.<br /> |pubmed-url=https://pubmed.ncbi.nlm.nih.gov/28825622<br /> |abstract=Investigators have dedicated considerable effort to understanding the molecular basis underlying Fanconi Anemia (FA), a rare human genetic disease featuring an extremely high incidence of cancer and many congenital defects. Among those studies, FA group D2 protein ([[FANCD2]]) has emerged as the focal point of FA signaling and plays crucial roles in multiple aspects of cellular life, especially in the cellular responses to DNA damage. Here, we discuss the recent and relevant studies to provide an updated review on the roles of [[FANCD2]] in the DNA damage response.<br /> |mesh-terms=* DNA Damage<br /> * DNA Repair<br /> * Fanconi Anemia<br /> * Fanconi Anemia Complementation Group D2 Protein<br /> * Humans<br /> * Signal Transduction<br /> |keywords=* DNA damage repair<br /> * FANCD2<br /> * Fanconi anemia<br /> * cancer and aging<br /> * checkpoint<br /> |full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578191<br /> }}</div>

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