TY - JOUR
T1 - Alternative mRNA splicing in three venom families underlying a possible production of divergent venom proteins of the habu snake, protobothrops flavoviridis
AU - Ogawa, Tomohisa
AU - Oda-Ueda, Naoko
AU - Hisata, Kanako
AU - Nakamura, Hitomi
AU - Chijiwa, Takahito
AU - Hattori, Shousaku
AU - Isomoto, Akiko
AU - Yugeta, Haruki
AU - Yamasaki, Shinichi
AU - Fukumaki, Yasuyuki
AU - Ohno, Motonori
AU - Satoh, Noriyuki
AU - Shibata, Hiroki
N1 - Funding Information:
Funding: This work was supported by Grants-in-Aid of MEXT, Japan (#25440214 and #18H02498 to H.S., #24651130 and #23107505 to T.O.), and by an Internal Fund to the Marine Genomics Unit, Okinawa Institute of Science and Technology Graduate University (OIST). This work was partly supported by the Cooperative Research Project Program of the Medical Institute of Bioregulation, Kyushu University (T.O., N.O.-U.).
Publisher Copyright:
© 2019 by the authors.
PY - 2019/10/9
Y1 - 2019/10/9
N2 - Snake venoms are complex mixtures of toxic proteins encoded by various gene families that function synergistically to incapacitate prey. A huge repertoire of snake venom genes and proteins have been reported, and alternative splicing is suggested to be involved in the production of divergent gene transcripts. However, a genome-wide survey of the transcript repertoire and the extent of alternative splicing still remains to be determined. In this study, the comprehensive analysis of transcriptomes in the venom gland was achieved by using PacBio sequencing. Extensive alternative splicing was observed in three venom protein gene families, metalloproteinase (MP), serine protease (SP), and vascular endothelial growth factors (VEGF). Eleven MP and SP genes and a VEGF gene are expressed as a total of 81, 61, and 8 transcript variants, respectively. In the MP gene family, individual genes are transcribed into different classes of MPs by alternative splicing. We also observed trans-splicing among the clustered SP genes. No other venom genes as well as non-venom counterpart genes exhibited alternative splicing. Our results thus indicate a potential contribution of mRNA alternative and trans-splicing in the production of highly variable transcripts of venom genes in the habu snake.
AB - Snake venoms are complex mixtures of toxic proteins encoded by various gene families that function synergistically to incapacitate prey. A huge repertoire of snake venom genes and proteins have been reported, and alternative splicing is suggested to be involved in the production of divergent gene transcripts. However, a genome-wide survey of the transcript repertoire and the extent of alternative splicing still remains to be determined. In this study, the comprehensive analysis of transcriptomes in the venom gland was achieved by using PacBio sequencing. Extensive alternative splicing was observed in three venom protein gene families, metalloproteinase (MP), serine protease (SP), and vascular endothelial growth factors (VEGF). Eleven MP and SP genes and a VEGF gene are expressed as a total of 81, 61, and 8 transcript variants, respectively. In the MP gene family, individual genes are transcribed into different classes of MPs by alternative splicing. We also observed trans-splicing among the clustered SP genes. No other venom genes as well as non-venom counterpart genes exhibited alternative splicing. Our results thus indicate a potential contribution of mRNA alternative and trans-splicing in the production of highly variable transcripts of venom genes in the habu snake.
KW - Metalloproteinase
KW - Serine protease
KW - Transcriptome variants
KW - Vascular endothelial growth factor
KW - Venom genes and proteins
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U2 - 10.3390/toxins11100581
DO - 10.3390/toxins11100581
M3 - Article
C2 - 31600994
AN - SCOPUS:85073118763
SN - 2072-6651
VL - 11
JO - Toxins
JF - Toxins
IS - 10
M1 - 581
ER -