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   <subfield code="a">Mouse/Human Sequence Divergence in a Region with a Paternal-Specific Methylation Imprint at the Human H19 Locus</subfield>
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   <subfield code="c">[Yoshihiro Jinno, Kazuo Sengoku, Mitsuyoshi Nakao, Kenichi Tamate, Toshinobu Miyamoto, Tetsuo Matsuzaka, James S. Sutcliffe, Tadashi Anan, Naoyuki Takuma, Kunihiko Nishiwaki, Yuichiro Ikeda, Tadayuki Ishimaru, Mutsuo Ishikawa, Norio Niikawa]</subfield>
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   <subfield code="a">We have identified a region with characteristics of a paternal-specific methylation imprint at the human H19 locus. This region, extending from −2.0 kb upstream to the start of transcription, is heavily methylated in sperm and on the paternal allele in somatic cells. This methylation was preserved during pre-implantation. Structural analysis revealed the presence of CpG islands and a large direct repeat with a 400 bp sequence reiterated several times, but no significant sequence homology to the corresponding region of the mouse H19 gene. These findings could suggest a role for secondary DNA structure in genomic imprinting across the species, and they also present a puzzling aspect of the evolution of the H19 regulatory region in human and mouse.</subfield>
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