Prediction of the Coding Sequences of Unidentified Human Genes. I. The Coding Sequences of 40 New Genes (KIAA0001-KIAA0040) Deduced by Analysis of Randomly Sampled cDNA Clones from Human Immature Myeloid Cell Line KG-1 (original) (raw)

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Institute of Gerontology, Nippon Medical School

Nakahara-ku, Kawasaki, Kanagawa 211, Japan

* To whom correspondence should be addressed. Tel. +81-44-733-5230; Fax. +81-44-733-5192

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Kazusa DNA Research Institute

Chuou-ku, Chiba 260, Japan

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Kazusa DNA Research Institute

Chuou-ku, Chiba 260, Japan

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Kazusa DNA Research Institute

Chuou-ku, Chiba 260, Japan

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Kazusa DNA Research Institute

Chuou-ku, Chiba 260, Japan

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Kazusa DNA Research Institute

Chuou-ku, Chiba 260, Japan

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Department of Biology, Faculty of Science, Nagoya University

Chigusa-ku, Nagoya 464, Japan

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Kazusa DNA Research Institute

Chuou-ku, Chiba 260, Japan

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Kazusa DNA Research Institute

Chuou-ku, Chiba 260, Japan

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Kazusa DNA Research Institute

Chuou-ku, Chiba 260, Japan

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Kazusa DNA Research Institute

Chuou-ku, Chiba 260, Japan

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Department of Biology, Faculty of Science, Nagoya University

Chigusa-ku, Nagoya 464, Japan

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Received:

30 October 1993

Published:

01 February 1994

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Nobuo Nomura, Nobuyuki Miyajima, Takashi Sazuka, Ayako Tanaka, Yutaka Kawarabayasi, Shusei Sato, Takahiro Nagase, Naohiko Seki, Ken-ichi Ishikawa, Satoshi Tabata, Prediction of the Coding Sequences of Unidentified Human Genes. I. The Coding Sequences of 40 New Genes (KIAA0001-KIAA0040) Deduced by Analysis of Randomly Sampled cDNA Clones from Human Immature Myeloid Cell Line KG-1, DNA Research, Volume 1, Issue 1, 1994, Pages 27–35, https://doi.org/10.1093/dnares/1.1.27
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Abstract

We established a protocol for the prediction of the coding sequences of unidentified human genes based on the double selection and sequence analysis of cDNA clones with inserts carrying unreported 5′-terminal sequences and with insert sizes corresponding to nearly full-length transcripts. By applying the protocol, cDNA clones with inserts longer than 2 kb were isolated from a cDNA library of human immature myeloid cell line KG-1, and the coding sequences of 40 new genes were predicted. A computer search of the sequences indicated that 20 genes contained sequences similar to known genes in the GenBank/EMBL databases. The sequences of the remaining 20 genes were entirely new, and characteristic protein motifs or domains were identified in 32 genes. Other sequence features noted were that the coding sequences of 23 genes were followed by relatively long stretches of 3′-untranslated sequences and that 5 genes contained repetitive sequences in their 3′-untranslated regions. The chromosomal location of these genes has been determined. By increasing the scale of the above analysis, the coding sequences of many unidentified genes can be predicted.

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Kazusa DNA Research Institute

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