Sequencing 5-Formyluracil in Genomic DNA at Single-Base Resolution
Albeit with low content, 5-formyluracil has been an important modification in genomic DNA. 5-formyluracil was found to be widely distributed among living bodies. Due to the equilibrium of keto-enol form, 5-formyluracil could be base-paired with guanine, thus inducing mutations in DNA. The highly reactive aldehyde group of 5-formyluracil could also cross-link with proteins nearby, preventing gene replication and expression. In certain cancerous tissues, the content of 5-formyluracil was found to be higher than the normal tissues adjacent to the tumor, and 5-formyluracil might be an important potential epigenetic mark. Nevertheless, the lack of a higher resolution sequencing technique has hampered the studies of 5-formyluracil. We adjusted the base-pairing of 5-formyluracil during the PCR amplification by changing the pH. Hence, we adopted the Alkaline Modulated 5-formyluracil Sequencing (AMfU-Seq), a single-base resolution analysis method, to profile 5-formyluracil at the genome scale. We analyzed the distribution of 5-formyluracil in the human thyroid carcinoma cells using AMfU-Seq. This technique can be used in the future investigations of 5-formyluracil.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2021 |
---|---|
Erschienen: |
2021 |
Enthalten in: |
Zur Gesamtaufnahme - volume:93 |
---|---|
Enthalten in: |
Analytical chemistry - 93(2021), 46 vom: 23. Nov., Seite 15445-15451 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Yang, Wei [VerfasserIn] |
---|
Links: |
---|
Themen: |
1195-08-0 |
---|
Anmerkungen: |
Date Completed 29.11.2021 Date Revised 29.11.2021 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1021/acs.analchem.1c03339 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM333135121 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM333135121 | ||
003 | DE-627 | ||
005 | 20231225221024.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2021 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1021/acs.analchem.1c03339 |2 doi | |
028 | 5 | 2 | |a pubmed24n1110.xml |
035 | |a (DE-627)NLM333135121 | ||
035 | |a (NLM)34775754 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Yang, Wei |e verfasserin |4 aut | |
245 | 1 | 0 | |a Sequencing 5-Formyluracil in Genomic DNA at Single-Base Resolution |
264 | 1 | |c 2021 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 29.11.2021 | ||
500 | |a Date Revised 29.11.2021 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Albeit with low content, 5-formyluracil has been an important modification in genomic DNA. 5-formyluracil was found to be widely distributed among living bodies. Due to the equilibrium of keto-enol form, 5-formyluracil could be base-paired with guanine, thus inducing mutations in DNA. The highly reactive aldehyde group of 5-formyluracil could also cross-link with proteins nearby, preventing gene replication and expression. In certain cancerous tissues, the content of 5-formyluracil was found to be higher than the normal tissues adjacent to the tumor, and 5-formyluracil might be an important potential epigenetic mark. Nevertheless, the lack of a higher resolution sequencing technique has hampered the studies of 5-formyluracil. We adjusted the base-pairing of 5-formyluracil during the PCR amplification by changing the pH. Hence, we adopted the Alkaline Modulated 5-formyluracil Sequencing (AMfU-Seq), a single-base resolution analysis method, to profile 5-formyluracil at the genome scale. We analyzed the distribution of 5-formyluracil in the human thyroid carcinoma cells using AMfU-Seq. This technique can be used in the future investigations of 5-formyluracil | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 7 | |a 5-formyluracil |2 NLM | |
650 | 7 | |a 1195-08-0 |2 NLM | |
650 | 7 | |a Uracil |2 NLM | |
650 | 7 | |a 56HH86ZVCT |2 NLM | |
650 | 7 | |a Guanine |2 NLM | |
650 | 7 | |a 5Z93L87A1R |2 NLM | |
650 | 7 | |a DNA |2 NLM | |
650 | 7 | |a 9007-49-2 |2 NLM | |
700 | 1 | |a Han, Shaoqing |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Xiong |e verfasserin |4 aut | |
700 | 1 | |a Wang, Yafen |e verfasserin |4 aut | |
700 | 1 | |a Zou, Guangrong |e verfasserin |4 aut | |
700 | 1 | |a Liu, Chaoxing |e verfasserin |4 aut | |
700 | 1 | |a Xu, Muxin |e verfasserin |4 aut | |
700 | 1 | |a Zhou, Xiang |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Analytical chemistry |d 1965 |g 93(2021), 46 vom: 23. Nov., Seite 15445-15451 |w (DE-627)NLM000025771 |x 1520-6882 |7 nnns |
773 | 1 | 8 | |g volume:93 |g year:2021 |g number:46 |g day:23 |g month:11 |g pages:15445-15451 |
856 | 4 | 0 | |u http://dx.doi.org/10.1021/acs.analchem.1c03339 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 93 |j 2021 |e 46 |b 23 |c 11 |h 15445-15451 |