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    <identifier>10.11922/sciencedb.o00019.00010</identifier>
    <datestamp>2022-02-09T15:23:24Z</datestamp>
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  <dc:date>2022-02-09</dc:date>
  <dc:title>Tissue RNA-seq expression data and results of venom LC-MS analysis for Hylyphantes graminicola</dc:title>
  <dc:identifier>doi:10.11922/sciencedb.o00019.00010</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Tissue RNA-seq expression data of all genes and results of venom LC-MS analysis from Hylyphantes graminicola (sheet-web spider) for manuscript &amp;quot;Chromosomal-level genome of a sheet-web spider provides insight into the composition and evolution of venom&amp;quot; were saved in this dataset.&amp;nbsp;we sequenced the transcriptomes of different tissues from H. graminicola, including the&amp;nbsp;venom gland, the brain, the&amp;nbsp;silk glands, the abdominal tissue with silk glands removed, and four pairs of legs. A total of 24 samples were used to generate the RNA-seq expression data. Total RNA was extracted using the RNAsimple Total RNA kit (TIANGEN, Beijing, China). PolyA RNA-sequencing (RNA-seq) libraries with an insert size of 250 bp were prepared and sequenced on the Illumina NovaSeq 6000 platform.Pooled sheet-web spider venom samples were reduced with DTT (10 mM, 60 min at 56&amp;deg;C), and alkylated with sufficient iodoacetamide (60 min at room temperature). The protein samples were then concentrated (20 min at 80 V) and separated (90 min at 120 V) in 12% SDS-PAGE gel electrophoresis. The gel was stained by Coomassie Brilliant Blue R-250 and decolored until the bands were visualized clearly. Trypsin treatment was performed at 37&amp;deg;C for 4 h. Peptides were washed three&amp;nbsp;times in 0.1% formic acid (FA) and 3% acetonitrile (ACN) and once in 0.1% FA and 70% ACN. The lyophilized samples were then dissolved in solution A (100% water and 0.1% FA) and injected into a homemade C18 Nano-Trap column (4.5 cm&amp;times;75 &amp;mu;m, 3 &amp;mu;m) at 55&amp;deg;C. The separated peptides were analyzed by Orbitrap Exploris 480 matched with FAIMS (Thermo Fisher), with an ion source of Nanospray Flex&amp;trade; (ESI), an ion transport capillary temperature of 320&amp;deg;C, and a spray voltage of 2.1 kV. The compensation voltage of FAIMS was set as -45 and -65, with a scan round time of 1 s, a resolution of 15,000, and an automatic gain control (AGC) target value of 750,000.</dc:description>
  <dc:subject>spider; Araneae; RNA-seq; LC-MS</dc:subject>
  <dc:creator>Bingyue Zhu</dc:creator>
  <dc:creator>Pengyu Jin</dc:creator>
  <dc:creator>Shuqiang Li</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:relation>http://www.doi.org/https://doi.org/10.1111/1755-0998.13601</dc:relation>
  <dc:publisher>Science Data Bank</dc:publisher>
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