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Molecular and Cellular Biology, February 2001, p. 1329-1335, Vol. 21, No. 4
0270-7306/01/$04.00+0   DOI: 10.1128/MCB.21.4.1329-1335.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Critical Role of Caenorhabditis elegans Homologs of Cds1 (Chk2)-Related Kinases in Meiotic Recombination

Isao Oishi,1,2 Kenji Iwai,1,2 Yukiko Kagohashi,3 Hiroko Fujimoto,1,2 Ken-Ichi Kariya,4 Tohru Kataoka,4 Hitoshi Sawa,5,6 Hideyuki Okano,5,7 Hiroki Otani,3 Hirohei Yamamura,1 and Yasuhiro Minami1,2,*

Department of Biochemistry,1 Department of Biomedical Regulation & Parasitology,2 and Department of Physiology,4 School of Medicine, Kobe University, Chuo-ku, Kobe 650-0017, Department of Anatomy, Shimane Medical University, Izumo 693-8501,3 Department of Neuroanatomy (D12), Graduate School of Medicine, Osaka University, Osaka 565-0871,5 and PREST (Precursory Research for Embryonic Science and Technology)6 and CREST (Core Research for Evolutional Science and Technology)7 of Japan Science and Technology Corporation (JST), Chiyoda-ku, Tokyo 102-0081, Japan

Received 14 August 2000/Returned for modification 14 September 2000/Accepted 13 November 2000

Although chromosomal segregation at meiosis I is the critical process for genetic reassortment and inheritance, little is known about molecules involved in this process in metazoa. Here we show by utilizing double-stranded RNA (dsRNA)-mediated genetic interference that novel protein kinases (Ce-CDS-1 and Ce-CDS-2) related to Cds1 (Chk2) play an essential role in meiotic recombination in Caenorhabditis elegans. Injection of dsRNA into adult animals resulted in the inhibition of meiotic crossing over and induced the loss of chiasmata at diakinesis in oocytes of F1 animals. However, electron microscopic analysis revealed that synaptonemal complex formation in pachytene nuclei of the same progeny of injected animals appeared to be normal. Thus, Ce-CDS-1 and Ce-CDS-2 are the first example of Cds1-related kinases that are required for meiotic recombination in multicellular organisms.


* Corresponding author. Mailing address: Department of Biomedical Regulation & Parasitology, Kobe University, School of Medicine, 7-5-1, Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan. Phone: 81-78-382-5560. Fax: 81-78-382-5579. E-mail: minami{at}kobe-u.ac.jp.


Molecular and Cellular Biology, February 2001, p. 1329-1335, Vol. 21, No. 4
0270-7306/01/$04.00+0   DOI: 10.1128/MCB.21.4.1329-1335.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



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