{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T01:04:57Z","timestamp":1791248697687,"version":"4.1.0"},"reference-count":65,"publisher":"The Company of Biologists","issue":"22","license":[{"start":{"date-parts":[[1997,11,15]],"date-time":"1997-11-15T00:00:00Z","timestamp":879552000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/www.biologists.com\/user-licence-1-1\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[1997,11,15]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n               <jats:p>Transcription factor E2F plays an important role in co-ordinating and integrating early cell cycle progression with the transcription apparatus. It is known that physiological E2F arises when a member of two families of proteins, E2F and DP, interact as E2F\/DP heterodimers and that transcriptional activity is regulated through the physical association of pocket proteins such as pRb. However, little information is available regarding the mechanisms which control the levels of functional E2F. In this study, we have characterised one such mechanism which regulates the nuclear accumulation and activity of E2F. Specifically, we show that E2F proteins fall into two distinct categories according to their ability to accumulate in nuclei, one being exemplified by E2F-1 and the other by E2F-4 and -5. Thus, E2F-1 possesses an intrinsic nuclear localization signal whereas E2F-4 and -5 are devoid of such a signal. Furthermore, we find for E2F-4 and -5 that two distinct processes govern their nuclear accumulation whereby the nuclear localization signal is supplied in trans from either a DP heterodimer partner or a physically associated pocket protein. It is consistent with the role of pocket proteins in regulating nuclear accumulation that we find E2F-5 to be nuclear during early cell cycle progression with an increased cytoplasmic concentration in cycling cells. Our data show that the mechanism of nuclear accumulation determines the functional consequence of E2F on cell cycle progression: pocket protein-mediated accumulation impedes cell cycle progression, whereas DP-regulated nuclear accumulation promotes cell cycle progression. Moreover, the inactivation of pocket proteins by the adenovirus E1a protein, and subsequent release of E2F, failed to displace nuclear E2F. Our study identifies a new level of regulation in the control of E2F activity exerted at the level of nuclear accumulation where subunit composition and interaction with pocket proteins dictates the functional consequence on cell cycle progression.<\/jats:p>","DOI":"10.1242\/jcs.110.22.2819","type":"journal-article","created":{"date-parts":[[2021,4,25]],"date-time":"2021-04-25T16:48:14Z","timestamp":1619369294000},"page":"2819-2831","source":"Crossref","is-referenced-by-count":41,"title":["Distinct mechanisms of nuclear accumulation regulate the functional consequence of E2F transcription factors"],"prefix":"10.1242","volume":"110","author":[{"given":"K. Elizabeth","family":"Allen","sequence":"first","affiliation":[{"name":"University of Glasgow, Glasgow 1 Division of Biochemistry and Molecular Biology, Davidson Building , , G12 8QQ, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Susana de la","family":"Luna","sequence":"additional","affiliation":[{"name":"University of Glasgow, Glasgow 1 Division of Biochemistry and Molecular Biology, Davidson Building , , G12 8QQ, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ron M.","family":"Kerkhoven","sequence":"additional","affiliation":[{"name":"2 Section of Molecular Carcinogenesis, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ren\u00e9","family":"Bernards","sequence":"additional","affiliation":[{"name":"2 Section of Molecular Carcinogenesis, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nicholas B. La","family":"Thangue","sequence":"additional","affiliation":[{"name":"University of Glasgow, Glasgow 1 Division of Biochemistry and Molecular Biology, Davidson Building , , G12 8QQ, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"237","published-online":{"date-parts":[[1997,11,15]]},"reference":[{"key":"2024010621450157800_JOCES_110_22_2819C1","doi-asserted-by":"publisher","first-page":"912","DOI":"10.1126\/science.2144057","article-title":"Suppression of human colorectal-carcinoma cell-growth by wild-type p53","volume":"249","author":"Baker","year":"1990","journal-title":"Science"},{"key":"2024010621450157800_JOCES_110_22_2819C2","doi-asserted-by":"publisher","first-page":"494","DOI":"10.1038\/351494a0","article-title":"Adenovirus Ela prevents the retinoblastoma gene product from complexing with a cellular transcription factor","volume":"351","author":"Bandara","year":"1991","journal-title":"Nature"},{"key":"2024010621450157800_JOCES_110_22_2819C3","doi-asserted-by":"publisher","first-page":"4317","DOI":"10.1002\/j.1460-2075.1993.tb06116.x","article-title":"Functional synergy between DP-1 and E2F-1 in the cell cycle-regulating transcription factor DRTF1\/E2F","volume":"13","author":"Bandara","year":"1993","journal-title":"EMBO J"},{"key":"2024010621450157800_JOCES_110_22_2819C4","doi-asserted-by":"publisher","first-page":"3104","DOI":"10.1002\/j.1460-2075.1994.tb06609.x","article-title":"DP-1: a cell cycle-regulated and phosphorylated component of transcription factor DRTF1\/E2F which is functionally important for recognition by pRb and the adenovirus E4 orf 6\/7 protein","volume":"13","author":"Bandara","year":"1994","journal-title":"EMBO J"},{"key":"2024010621450157800_JOCES_110_22_2819C5","doi-asserted-by":"publisher","first-page":"2680","DOI":"10.1101\/gad.8.22.2680","article-title":"E2F-4, a new member of the E2F gene family, has oncogenic activity and associates with p107 in vivo","volume":"8","author":"Beijersbergen","year":"1994","journal-title":"Genes Dev"},{"key":"2024010621450157800_JOCES_110_22_2819C6","doi-asserted-by":"publisher","first-page":"3401","DOI":"10.1128\/MCB.16.7.3401","article-title":"Cell cycle regulation of the murine cyclin E gene depends on an E2F binding site in the promoter","volume":"16","author":"Botz","year":"1996","journal-title":"Mol. 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